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Human Genome Region REGION113

Assembly:
GRCh38.p14
Location:
chr2:728,878-860,300
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270770.1 NT_187525.1 ALT Unavailable Unavailable Unavailable
           

REGION113 -- chr2 (CM000664.2):728,878-860,300