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Human Genome Region REGION167

Assembly:
GRCh38.p14
Location:
chr13:89,598,964-89,764,093
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270841.1 NT_187595.1 ALT Unavailable Unavailable Unavailable
           

REGION167 -- chr13 (CM000675.2):89,598,964-89,764,093