[];P{wHy}CG4996DG14810
Map location is based on alignment to the reference genome of genomic sequence flanking a transposable element insertion.
The P{wHy}CG4996DG14810 insertion has been mobilised, resulting in the P{3'wHy}CG499614H10Y-53 insertion and a proximally extending genomic disruption, which is most likely a simple 123,132bp deletion.