Human Genome Region NOR_CHR_22
- Assembly:
- GRCh38.p14
- Location:
- chr22:10,097,632-10,510,000
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| ML143380.1 | NW_021160026.1 | FIX | Unavailable | Unavailable | Unavailable | |