Human Genome Region ZNF66
- Assembly:
- GRCh38.p14
- Location:
- chr19:20,663,141-21,042,381
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| GL383573.1 | NW_003315962.1 | ALT | Unavailable | Unavailable | Unavailable | |