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Human Genome Region REGION181

Assembly:
GRCh38.p14
Location:
chr20:63,414,721-63,471,095
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270871.1 NT_187625.1 ALT Unavailable Unavailable Unavailable
           

REGION181 -- chr20 (CM000682.2):63,414,721-63,471,095