Human Genome Region SAMD1
- Assembly:
- GRCh38.p13
- Location:
- chr19:13,788,160-14,281,006
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| ML143376.1 | NW_021160022.1 | FIX | 493,165 | 0 | 318 | |