Known variations to the primary assembly, due to variability in the human genome sequence (eg. the highly variable MHC locus containing halpotypes HSCHR6_MHC_COX, HSCHR6_MHC_SSTO, HSCHR6_MHC_APD, HSCHR6_MHC_DBB, HSCHR6_MHC_MANN, HSCHR6_MHC_MCF, and HSCHR6_MHC_QBL). In Region in Detail, the haplotype regions are coloured with a red background.

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