Human Genome Region SPATC1L
- Assembly:
- GRCh38.p14
- Location:
- chr21:46,140,942-46,221,322
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KI270872.1 | NT_187626.1 | ALT | Unavailable | Unavailable | Unavailable | |