nsv6315380
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:582,080
- Description:GRCh37/hg19 Xq25(chrX:122855926-123438005) AND Xq25 microduplication syndrome