Human Genome Region SNTB2
- Assembly:
- GRCh38.p14
- Location:
- chr16:69,140,151-69,224,690
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| GL383557.1 | NW_003315946.1 | ALT | Unavailable | Unavailable | Unavailable | |