Human Genome Region REGION199
- Assembly:
- GRCh38.p14
- Location:
- chr1:210,220,259-210,677,001
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KN538360.1 | NW_011332687.1 | FIX | Unavailable | Unavailable | Unavailable | |