Human Genome Region REGION162
- Assembly:
- GRCh38.p14
- Location:
- chr12:130,323,076-130,394,967
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KI270833.1 | NT_187589.1 | ALT | Unavailable | Unavailable | Unavailable | |