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Human Genome Region IGH

Assembly:
GRCh38.p14
Location:
chr14:92,885,439-94,394,539
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270847.1 NT_187601.1 ALT Unavailable Unavailable Unavailable
           

IGH -- chr14 (CM000676.2):92,885,439-94,394,539