Human Genome Region ZNF66
- Assembly:
- GRCh37.p13
- Location:
- chr19:20,845,947-21,225,187
- 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 | NOVEL | 385,657 | 1,093 | 7,153 | |