Human Genome Region REGION222
- Assembly:
- GRCh38.p14
- Location:
- chr4:14,931,450-15,019,028
- Cytogenetic location:
No associated genome issues
Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
---|---|---|---|---|---|---|
KQ090013.1 | NW_013171799.1 | NOVEL | Unavailable | Unavailable | Unavailable | |