Skip navigation and go to main content

Human Genome Region REGION218

Assembly:
GRCh38.p14
Location:
chr13:84,294,441-84,452,423
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KQ090024.1 NW_013171810.1 NOVEL Unavailable Unavailable Unavailable
           

REGION218 -- chr13 (CM000675.2):84,294,441-84,452,423