Human Genome Region REGION192
- Assembly:
- GRCh38.p14
- Location:
- chr3:44,474,647-44,925,818
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KN196475.1 | NW_009646197.1 | FIX | Unavailable | Unavailable | Unavailable | |