Skip navigation and go to main content

Human Genome Region REGION19

Assembly:
GRCh38.p14
Location:
chr11:25,170,407-25,319,080
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383547.1 NW_003315936.1 ALT Unavailable Unavailable Unavailable
           

REGION19 -- chr11 (CM000673.2):25,170,407-25,319,080