Skip navigation and go to main content

Human Genome Region GPI

Assembly:
GRCh38.p14
Location:
chr19:34,350,807-34,392,977
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270866.1 NT_187619.1 ALT Unavailable Unavailable Unavailable
           

GPI -- chr19 (CM000681.2):34,350,807-34,392,977