Human Genome Region SH2B2
- Assembly:
- GRCh37.p13
- Location:
- chr7:101,718,951-102,072,447
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| GL582968.1 | NW_003571037.1 | FIX | 356,330 | 166 | 2,932 | |