Skip navigation and go to main content

Human Genome Region REGION21

Assembly:
GRCh37.p13
Location:
chr12:28,148,967-28,263,711
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383549.1 NW_003315938.1 NOVEL 120,804 54 6,086
           

REGION21 -- chr12 (NC_000012.11):28,148,967-28,263,711