Human Genome Region REGION139
- Assembly:
- GRCh38.p12
- Location:
- chr6:65,774,814-65,944,033
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KI270800.1 | NT_187555.1 | ALT | 175,808 | 93 | 6,647 | |