Human Genome Region REGION2
- Assembly:
- GRCh38.p13
- Location:
- chr1:153,700,531-153,865,738
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| GL383518.1 | NW_003315905.1 | ALT | 182,439 | 49 | 17,291 | |