Human Genome Region REGION219
- Assembly:
- GRCh38.p14
- Location:
- chr13:108,604,134-108,722,945
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KQ090025.1 | NW_013171811.1 | NOVEL | Unavailable | Unavailable | Unavailable | |