Human Y-chromosome DNA haplogroup
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In human genetics, a human Y-chromosome DNA haplogroup is a haplogroup defined by differences in the non-recombining portions of DNA from the Y chromosome (called Y-DNA). It represents human genetic diversity based on single-nucleotide polymorphisms (SNPs) on the Y chromosome.
Y-DNA haplogroups represent major branches of the Y-chromosome phylogenetic tree. Y-chromosomal Adam is the name given by researchers to the patrilineal most recent common ancestor of all living humans at the root of this tree. Estimates of the date when Y-chromosomal Adam lived have varied significantly in different studies. Archaeological and genetic data suggest that the source populations of Paleolithic humans survived the glacial maxima (including the LGM) and human Y-DNA haplogroups emerged in sparsely wooded refugia, and dispersed through areas of high primary productivity while avoiding dense forest cover.
- 1 Naming convention
- 2 Phylogenetic structure
- 3 Major Y-DNA haplogroups
- 3.1 Haplogroups A & B
- 3.2 Haplogroup CT (P143)
- 3.3 Haplogroup C (M130)
- 3.4 Haplogroup F (M89)
- 3.5 Haplogroup D (M174)
- 3.6 Haplogroup E (M96)
- 3.7 Haplogroup G (M201)
- 3.8 Haplogroup H (M69)
- 3.9 Haplogroup I (M170)
- 3.10 Haplogroup J (M304)
- 3.11 Haplogroup K (M9)
- 3.12 Haplogroups L & T (K1)
- 3.13 Haplogroup K2 (K-M526)
- 3.14 Haplogroups K2a, K2a1, NO & NO1
- 3.15 Haplogroup N
- 3.16 Haplogroup O
- 3.17 Haplogroups K2b1, M & S
- 3.18 Haplogroup P (K2b2)
- 3.19 Haplogroup Q M242
- 3.20 Haplogroup R (M207)
- 4 Chronological development of haplogroups
- 5 See also
- 6 References
- 7 Further reading
- 8 External links
Y-DNA haplogroups are defined by the presence of a series of Y-DNA SNP markers. Subclades are defined by a terminal SNP, the SNP furthest down in the Y-chromosome phylogenetic tree. The Y Chromosome Consortium (YCC) developed a system of naming major Y-DNA haplogroups with the capital letters A through T, with further subclades named using numbers and lower case letters (YCC longhand nomenclature). YCC shorthand nomenclature names Y-DNA haplogroups and their subclades with the first letter of the major Y-DNA haplogroup followed by a dash and the name of the defining terminal SNP.
Y-DNA haplogroup nomenclature is changing over time to accommodate the increasing number of SNPs being discovered and tested, and the resulting expansion of the Y-chromosome phylogenetic tree. This change in nomenclature has resulted in inconsistent nomenclature being used in different sources. This inconsistency, and increasingly cumbersome longhand nomenclature, has prompted a move towards using the simpler shorthand nomenclature. In September 2012, Family Tree DNA provided the following explanation of its changing Y-DNA haplogroup nomenclature to individual customers on their Y-DNA results pages (note that the haplogroup mentioned below relates to a specific individual):
Long time customers of Family Tree DNA have seen the YCC-tree of Homo Sapiens evolve over the past several years as new SNPs have been discovered. Sometimes these new SNPs cause a substantial change in the "longhand" explanation of your terminal Haplogroup. Because of this confusion, we introduced a shorthand version a few years ago that lists the branch of the tree and your terminal SNP, i.e. J-L147, in lieu of J1c3d. Therefore, in the very near term, Family Tree DNA will discontinue showing the current "longhand" on the tree and we will focus all of our discussions around your terminal defining SNP.
This changes no science – it just provides an easier and less confusing way for us all to communicate.
Major Y-DNA haplogroups
Haplogroups A & B
Using fast evolving SNPs, haplogroup A is the macrohaplogroup from which all modern paternal haplogroups descend. It is sparsely distributed in Africa. BT is a subclade of haplogroup A; more precisely of A1b (A2-T in Cruciani et al. 2011), as follows:
- Haplogroup A
Haplogroup CT (P143)
The defining mutations separating CT (all haplogroups excepting A and B) are M168 and M294. These mutations predate the "Out of Africa" migration. The defining mutations of DE probably occurred in Northeastern Africa some 65,000 years ago. The P143 mutation that defines Haplogroup CF may have occurred at that time, bringing modern humans to the southern coast of Asia.
- Haplogroup CF (P143) Found outside of Africa, throughout Eurasia, Oceania, and the Americas
- Haplogroup DE (M1, M145, M203) ca. 65 ka
Haplogroup C (M130)
- Haplogroup C (M130, M216) Found in Asia, Oceania, and North America
- Haplogroup C1 (F3393/Z1426)
- Haplogroup C1a (CTS11043)
- Haplogroup C1b (F1370, Z16480)
- Haplogroup C1b1 (AM00694/K281)
- Haplogroup C1b2 (B477/Z31885)
- Haplogroup C2 (M217, P44) Found throughout Eurasia and North America, but especially among Mongols, Kazakhs, Tungusic peoples, Paleosiberians, and Na-Dené-speaking peoples
- Haplogroup C1 (F3393/Z1426)
Haplogroup F (M89)
The groups descending from haplogroup F are found in some 90% of the world's population, but almost exclusively outside of sub-Saharan Africa.
F xG,H,I,J,K is rare in modern populations and peaks in South Asia, especially Sri Lanka. It also appears to have long been present in South East Asia. has been reported at rates of 4-5% in Sulawesi and Lembata. One study, which did not comprehensively screen for other subclades of F-M89 (including some subclades of GHIJK), found that Indonesian men with the SNP P14/PF2704 (which is equivalent to M89), comprise 1.8% of men in West Timor, 1.5% of Flores 5.4% of Lembata 2.3% of Sulawesi and 0.2% in Sumatra. F* (F xF1,F2,F3) has been reported among 10% of males in Sri Lanka and South India, 5% in Pakistan, as well as lower levels among the Tamang people (Nepal), and in Iran. F1 (P91), F2 (M427) and F3 (M481; previously F5) are all highly rare and virtually exclusive to regions/ethnic minorities in Sri Lanka, India, Nepal, South China, Thailand, Burma, and Vietnam.In such cases, however, the possibility of misidentification is considered to be relatively high and some may belong to misidentified subclades of Haplogroup GHIJK.
Haplogroup D (M174)
- Haplogroup D (M174) Found in Japan, China (especially Tibet), the Andaman Islands
- D1 (CTS11577)
- D1a (Z27276, Z27283, Z29263)
- Haplogroup D1b (M55, M57, M64.1, M179, P12, P37.1, P41.1 (M359.1), 12f2.2) Found mainly in Japan
- D2 (L1366, L1378, M226.2) Found in Mactan Island, Philippines
- D1 (CTS11577)
Haplogroup E (M96)
- Haplogroup E (M40, M96) Found primarily in Africa
- Haplogroup E1 (P147)
- Haplogroup E1a (M33, M132) formerly E1
- Haplogroup E1b (P177)
- Haplogroup E2 (M75)
- Haplogroup E1 (P147)
Haplogroup G (M201)
It is found in many ethnic groups in Eurasia; most common in the Caucasus, Iran, Anatolia and the Levant. Found in almost all European countries, but most common in Gagauzia, southeastern Romania, Greece, Italy, Spain, Portugal, Tyrol, and Bohemia with highest concentrations on some Mediterranean islands; uncommon in Northern Europe.
- Haplogroup G1
- Haplogroup G2
Haplogroup H (M69)
Haplogroup H (M69) probably emerged in South Asia, about 30,000 to 40,000 years BP, and remains prevalent there, in the forms of H1 (M69) and H3 (Z5857).
Haplogroup I (M170)
- Haplogroup I1 (M253) Found mainly in northern Europe
- Haplogroup I2 (P215) Found mainly in southeast Europe and Sardinia save for I2B1 (m223) which is primarily found in Western, Central, and Northern Europe.
Haplogroup J (M304)
- Haplogroup J* (J-M304*) is rare outside the island of Socotra.
Haplogroup K (M9)
Haplogroups L & T (K1)
Haplogroup L (M20) is found in South Asia, Central Asia, South-West Asia, and the Mediterranean.
Haplogroup T (M184, M70, M193, M272) is found at high levels in the Horn of Africa (mainly Afro-Asiatic-speaking peoples), parts of South Asia, the Middle East, and the Mediterranean. T-M184 is also found in significant minorities of Sciaccensi, Stilfser, Fulbe, Egyptians, Omanis, Sephardi Jews, and Ibizans (Eivissencs). It is also found at low frequencies in other parts of the Mediterranean and South Asia.
Haplogroup K2 (K-M526)
The only living males reported to carry the basal paragroup K2* are indigenous Australians. Major studies published in 2014 and 2015 suggest that up to 27% of Aboriginal Australian males carry K2*, while others carry a subclade of K2.
Haplogroups K2a, K2a1, NO & NO1
Haplogroup N possibly originated in eastern Asia and spread both west into Siberia and north, being the most common group found in some Uralic speaking peoples. Haplogroup O is found at its highest frequency in East Asia and Southeast Asia, with lower frequencies in the South Pacific, Central Asia, and South Asia.
Haplogroup O (M175) is found in East Asia, Southeast Asia, and the South Pacific.
- Haplogroup O1 (F265/M1354, CTS2866, F75/M1297, F429/M1415, F465/M1422)
- Haplogroup O1a (M119, CTS31, F589/Page20, L246, L466) Found in eastern and southern China, Taiwan, and Southeast Asia, especially among Austronesian and Tai–Kadai peoples
- Haplogroup O1b (P31, M268)
- Haplogroup O2 (M122) Found throughout East Asia, Southeast Asia, and Austronesia including Polynesia
Haplogroups K2b1, M & S
Its primary subclades are two major haplogroups:
- Haplogroup S (B254) also known as K2b1a: found in the highlands of Papua New Guinea and;
- Haplogroup M (P256) also known as K2b1b: found in New Guinea and Melanesia.
Haplogroup P (K2b2)
P*, P1* and P2 are found together only on the island of Luzon, in The Philippines. In particular, P* and P1* are found at significant rates among members of the Aeta (or Agta) people of Luzon. While, P1* is now more common among living individuals in Eastern Siberia and Central Asia, it is also found at low levels in mainland South East Asia and South Asia. Considered together, these distributions tend to suggest that P* emerged from K2b in South East Asia.
P1 is also the parent node of two primary clades:
- Haplogroup Q (Q-M242) and;
- Haplogroup R (R-M207). These share the common marker M45 in addition to at least 18 other SNPs.
Haplogroup Q M242
Q is defined by the SNP M242. It is believed to have arisen in Central Asia approximately 17,000 to 22,000 years ago. The subclades of Haplogroup Q with their defining mutation(s), according to the 2008 ISOGG tree are provided below. ss4 bp, rs41352448, is not represented in the ISOGG 2008 tree because it is a value for an STR. This low frequency value has been found as a novel Q lineage (Q5) in Indian populations
The 2008 ISOGG tree
- Q (M242)
- Q1 (P36.2)
- Q1a (MEH2)
- Q1a1 (M120, M265/N14) Found with low frequency among Dungans, Han Chinese, Hazaras, Japanese, Koreans, and Tibetans
- Q1a2 (M25, M143) Found at low to moderate frequency among some populations of Southwest Asia, Central Asia, and Siberia
- Q1a3 (M346)
- Q1a4 (P48)
- Q1a5 (P89)
- Q1a6 (M323) Found in a significant minority of Yemeni Jews
- Q1b (M378) Found at low frequency among samples of Hazara and Sindhis
Haplogroup R (M207)
Haplogroup R is defined by the SNP M207. The bulk of Haplogroup R is represented in descendant subclade R1, which likely originated on the Eurasian Steppes. R1 has two descendant subclades: R1a and R1b.
Haplogroup R1b is the dominant haplogroup of Western Europe and also found sparsely distributed among various peoples of Asia and Africa. Its subclade R1b1a2 (M269) is the haplogroup that is most commonly found among modern Western European populations, and has been associated with the Italo-Celtic and Germanic peoples.
- Haplogroup R1 (M173) Found throughout western Eurasia
- Haplogroup R2 (M124) Found in South Asia, Caucasus, Central Asia, and Eastern Europe
Chronological development of haplogroups
|Haplogroup||Possible time of origin||Possible place of origin||Possible TMRCA|
|A00||192–307,000 years ago|
|E||50-55,000 years ago||East Africa or Asia||27-59,000 years ago|
|F||38-56,000 years ago|
|IJ||30-46,000 years ago|
|K||40-54,000 years ago|
|E-M215 (E1b1b)||31-46,000 years ago||39-55,000 years ago|
|P||27-41,000 years ago|
|J||19-44,500 years ago|
|R||20-34,000 years ago|
|I||15-30,000 years ago|
|R-M173 (R1)||13-26,000 years ago|
|I-M438 (I2)||28-33,000 years ago||16,000-20,000 years ago|
|E-M35||20,000-30,000 years ago||15–21,000 years ago|
|J-M267 (J1)||15-34,000 years ago|
|R-M420 (R1a)||22,000 years ago||8-10,000 years ago|
|R-M343 (R1b)||22,000 years ago||West Asia|
|N||at least 21,000 years ago (STR age)|
|I-M253 (I1)||11-21,000 or 28-33,000 years ago||3-5,000 years ago|
|J-M172 (J2)||15,000-22,000 years ago||19-24,000 years ago|
|E-M78||15-20,000 or 17,500-20,000 years ago||Northeast Africa||at least 17,000 years ago|
|E-V12||12,500-18,000 years ago|
|R-M17||13 ,000 or 18,000 years ago||India|
|I-L460 (I2a)||present 13,000 years ago|
|I-M223||11-18,000 years ago|
|E-V13||7-17,000 years ago||West Asia||4,000-4,700 years ago (Europe)
6,800-17,000 years ago (Asia)
|R-Z280||11-14,000 years ago|
|N-M46 (N1c1)||at least 12,000 years ago (STR age)|
|R-M458||11,000 years ago|
|I-P37||6-16,000, present 10,000 years ago|
|I-M423 (I2a1b)||present 10,000 years ago|
|I-M26 (I2a1a)||2-17,000, present 8,000 years ago|
|R-M269||5,500-8,000 years ago|
|R-L11, R-S116||3-5,000 years ago|
- Y-chromosome haplogroups in populations of the world
- Y-DNA haplogroups in populations of Europe
- Genetic history of Europe
- List of Y-DNA single-nucleotide polymorphisms
- List of Y-STR markers
- Human mitochondrial DNA haplogroups
- * (haplogroup)
- Molecular phylogeny
- Genetic genealogy
- Genealogical DNA test
- Conversion table for Y chromosome haplogroups
|Evolutionary tree of human Y-chromosome DNA haplogroups [χ 1][χ 2]|
|A00||A0-T [χ 3]|
|I||J||LT [χ 5]||K2|
|L||T||NO [χ 6]||K2b [χ 7]||K2c||K2d||K2e [χ 8]|
|N||O||K2b1 [χ 9]||P|
|M||S [χ 10]||Q||R|
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|Wikimedia Commons has media related to Human Y-DNA haplogroups.|
- ISOGG Y-DNA Haplogroup Tree
- FTDNA (2008) Y-Chromosome Phylogenetic Tree
- Chart of the speed of different Y chromosomal STR mutation rates
- Map of Y Haplogroups
- Atlas of the Human Journey, from the Genographic Project, National Geographic
- DNA Heritage's Y-haplogroup map
- Video tutorial on Discovering Paternal Ancestry with Y-Chromosomes
- Haplogroup Predictor
- Semino O, Passarino G, Oefner PJ, et al. (November 2000). "The genetic legacy of Paleolithic Homo sapiens sapiens in extant Europeans: a Y chromosome perspective". Science. 290 (5494): 1155–9. doi:10.1126/science.290.5494.1155. PMID 11073453.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles> As PDF Paper that defined "Eu" haplogroups
- Y-DNA Haplogroup and Sub-clade Projects
- Kerchner's YDNA Haplogroup Descriptions, Projects & Links
- Y-DNA Testing Company STR Marker Comparison Chart
- Y-DNA Ethnographic and Genographic Atlas and Open-Source Data Compilation
- Y Chromosome Consortium