Skip navigation and go to main content

Human Genome Region NOR_CHR_14

Assembly:
GRCh38.p14
Location:
chr14:15,600,817-16,000,000
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
ML143367.1 NW_021160013.1 FIX Unavailable Unavailable Unavailable
           

NOR_CHR_14 -- chr14 (CM000676.2):15,600,817-16,000,000