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Human Genome Region REGION118

Assembly:
GRCh38.p14
Location:
chr2:116,874,515-116,981,849
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270771.1 NT_187530.1 ALT Unavailable Unavailable Unavailable
           

REGION118 -- chr2 (CM000664.2):116,874,515-116,981,849