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Human Genome Region REGION122

Assembly:
GRCh38.p14
Location:
chr3:20,277,967-20,382,602
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270783.1 NT_187535.1 ALT Unavailable Unavailable Unavailable
           

REGION122 -- chr3 (CM000665.2):20,277,967-20,382,602