Human Genome Region REGION99
- Assembly:
- GRCh38.p14
- Location:
- chr6:168,796,076-168,951,646
- Cytogenetic location:
No associated genome issues
Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
---|---|---|---|---|---|---|
KB021644.2 | NW_004166862.2 | ALT | Unavailable | Unavailable | Unavailable | |