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Human Genome Region REGION21

Assembly:
GRCh38.p14
Location:
chr12:27,996,034-28,110,778
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 ALT Unavailable Unavailable Unavailable
           

REGION21 -- chr12 (CM000674.2):27,996,034-28,110,778