Human Genome Region REGION182
- Assembly:
- GRCh38.p14
- Location:
- chr21:17,146,893-17,310,433
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KI270874.1 | NT_187628.1 | ALT | Unavailable | Unavailable | Unavailable | |