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Human Genome Region NOR_CHR_13

Assembly:
GRCh38.p14
Location:
chr13:15,590,088-16,000,000
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
ML143366.1 NW_021160012.1 FIX Unavailable Unavailable Unavailable
           

NOR_CHR_13 -- chr13 (CM000675.2):15,590,088-16,000,000