Human Genome Region PRADER_WILLI
- Assembly:
- GRCh38.p14
- Location:
- chr15:19,775,255-24,552,710
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KI270848.1 | NT_187603.1 | ALT | Unavailable | Unavailable | Unavailable | |
| KI270851.1 | NT_187604.1 | ALT | Unavailable | Unavailable | Unavailable | |
| KI270852.1 | NT_187602.1 | ALT | Unavailable | Unavailable | Unavailable | |
| KI270906.1 | NT_187659.1 | ALT | Unavailable | Unavailable | Unavailable | |
| ML143371.1 | NW_021160017.1 | FIX | Unavailable | Unavailable | Unavailable | |