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Human Genome Region REGION187

Assembly:
GRCh38.p14
Location:
chrX:319,338-601,516
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270880.1 NT_187634.1 ALT Unavailable Unavailable Unavailable
KI270913.1 NT_187667.1 ALT Unavailable Unavailable Unavailable
           

REGION187 -- chrX (CM000685.2):319,338-601,516