Human Genome Region SHANK2
- Assembly:
- GRCh37.p13
- Location:
- chr11:70,301,893-71,088,948
- Cytogenetic location:
No associated genome issues
Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
---|---|---|---|---|---|---|
JH806581.1 | NW_004070871.1 | FIX | 872,115 | 15 | 35,105 | |