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Human Genome Region PAM16

Assembly:
GRCh38.p14
Location:
chr16:4,299,637-4,530,534
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270855.1 NT_187608.1 ALT Unavailable Unavailable Unavailable
           

PAM16 -- chr16 (CM000678.2):4,299,637-4,530,534