nsv6313619
- 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:12,537,799
- Description:GRCh37/hg19 2p23.2-21(chr2:29899368-42441440) AND not specified