Human Genome Region FAM101B
- Assembly:
- GRCh37.p13
- Location:
- chr17:252,429-296,626
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| GL383562.1 | NW_003315951.1 | FIX | 45,551 | 0 | 1,353 | |