Skip navigation and go to main content

Human Genome Region MEGF11

Assembly:
GRCh37.p12
Location:
chr15:66,200,521-66,577,156
Cytogenetic location:

Loading ideogram...

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383555.1 NW_003315944.1 NOVEL 388,773 47 12,158
           

MEGF11 -- chr15 (NC_000015.9):66,200,521-66,577,156