Human Genome Region REGION239
- Assembly:
- GRCh38.p14
- Location:
- chrX:4,950,957-5,129,468
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KV766199.1 | NW_017363820.1 | NOVEL | Unavailable | Unavailable | Unavailable | |