nsv4683913 - (obsolete)
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:
- Submitted on:GRCh37
- Variant Calls:0
- Validation:Not tested
- Clinical Assertions: No
- Region Size:15,276
- Description:NC_000019.10:g.(?_11116084)_(11131359_?)del AND Familial hypercholesterolemia
Source: NCBI
This variant has been obsoleted and is no longer valid.