Human Genome Region REGION69
- Assembly:
- GRCh37.p13
- Location:
- chr17:77,412,077-77,766,016
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| JH591186.1 | NW_003871089.1 | FIX | 376,223 | 280 | 106,481 | |