Human Genome Region REGION9
- Assembly:
- GRCh37.p13
- Location:
- chr5:12,681,538-12,744,122
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| GL383532.1 | NW_003315920.1 | NOVEL | 82,728 | 41 | 20,178 | |