Human Genome Region REGION190
- Assembly:
- GRCh38.p14
- Location:
- chr1:112,909,422-113,029,606
- Cytogenetic location:
No associated genome issues
Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
---|---|---|---|---|---|---|
KN196474.1 | NW_009646196.1 | FIX | Unavailable | Unavailable | Unavailable | |