Human Genome Region REGION226
- Assembly:
- GRCh38.p14
- Location:
- chr9:8,983,671-9,142,737
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KQ090018.1 | NW_013171804.1 | NOVEL | Unavailable | Unavailable | Unavailable | |