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Human Genome Region REGION4

Assembly:
GRCh37.p13
Location:
chr2:36,453,102-36,590,458
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383521.1 NW_003315908.1 NOVEL 143,390 74 6,100
           

REGION4 -- chr2 (NC_000002.11):36,453,102-36,590,458