Human Genome Region REGION99
- Assembly:
- GRCh37.p13
- Location:
- chr6:169,194,170-169,351,741
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KB021644.1 | NW_004166862.1 | NOVEL | 187,824 | 96 | 30,274 | |