Human Genome Region INTS4L2
- Assembly:
- GRCh37.p13
- Location:
- chr7:65,012,083-65,286,677
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KE332499.1 | NW_004775430.1 | FIX | 274,521 | 137 | 51 | |