Human Genome Region PTEN
- Assembly:
- GRCh38.p14
- Location:
- chr10:87,784,179-88,048,756
- Cytogenetic location:
No associated genome issues
Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
---|---|---|---|---|---|---|
KQ090021.1 | NW_013171807.1 | FIX | Unavailable | Unavailable | Unavailable | |