Human Genome Region CT47_REGION
- Assembly:
- GRCh38.p14
- Location:
- chrX:120,599,933-121,083,725
- Cytogenetic location:
No associated genome issues
Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
---|---|---|---|---|---|---|
ML143381.1 | NW_021160027.1 | FIX | Unavailable | Unavailable | Unavailable | |