[];P{wHy}eIF3-S8DG14606
Map location is based on alignment to the reference genome of genomic sequence flanking a transposable element insertion.
The P{wHy}eIF3-S8DG14606 insertion has been mobilised, resulting in the P{3'wHy}eIF3-S814F06Y-28 insertion and a proximally extending genomic disruption, which is most likely a simple 49,073bp deletion.