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Human Genome Region IGH

Assembly:
GRCh37.p13
Location:
chr14:105,803,171-107,268,434
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KB021645.1 NW_004166863.1 FIX 1,523,386 3,357 96,922
           

IGH -- chr14 (NC_000014.8):105,803,171-107,268,434