Human Genome Region REGION168
- Assembly:
- GRCh38.p14
- Location:
- chr13:112,182,875-112,505,943
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KI270838.1 | NT_187592.1 | ALT | Unavailable | Unavailable | Unavailable | |