Haplogroup K (defined by the M9 mutation) is the one of the major Eurasian Y-Choromosome lineage, descending from the the borader CT haplogroup with the early migration of modern humans out of Africa.[1] Descendant lineages of Y-chromosome haplogroup K are widespread across Eurasia. Haplogroup K2a/O is the dominant paternal lineage in East and Southeast Asia, while haplogroup N reaches high frequencies in parts of northern Eurasia and eastern Europe, where it appears to have expanded westward from inner Asia and southern Siberia.[2][3]
The K2b-derived haplogroups R and Q are among the major paternal lineages in Europe, Central Asia, and the Americas, and Q is also the principal Native American Y-chromosome haplogroup with related lineages found in Siberia. [4]
In South Asia, the main paternal lineages include R1, R2, L, O, H, J2 and C, which together account for most Y-chromosome diversity; K2a/O-M175 is especially common in some northeastern and Tibeto-Burman/Austroasiatic-speaking populations.[5] Haplogroup J1 peaks in the Arabian Peninsula, southern Mesopotamia, and the southern Levant,[6] whereas the African subclade K2b/R1b-V88 has been reported in parts of central-western Africa and is often interpreted as evidence of a back-to-Africa migration.[7]
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