Human Genome Region REGION89
- Assembly:
- GRCh37.p13
- Location:
- chrX:71,530,834-72,366,730
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| JH806592.1 | NW_004070882.1 | FIX | 835,911 | 161 | 561 | |