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Human Genome Region SMA

Assembly:
GRCh38
Location:
chr5:69,216,819-71,614,443
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL339449.2 NW_003315917.2 ALT 1,612,928 2,239 51,086
KI270897.1 NT_187651.1 ALT 1,144,418 1,378 28,939
           

SMA -- chr5 (NC_000005.10):69,216,819-71,614,443