Human Genome Region REGION119
- Assembly:
- GRCh38.p14
- Location:
- chr2:131,697,037-131,806,107
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KI270768.1 | NT_187528.1 | ALT | Unavailable | Unavailable | Unavailable | |