nsv4346691 - (obsolete)
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:
- Submitted on:GRCh37 (hg19)
- Variant Calls:0
- Validation:Not tested
- Clinical Assertions: No
- Region Size:4,270
- Description:NM_000527.4(LDLR):c.1891_2311+1062del (p.(?)) AND Familial hypercholesterolemia 1
Source: NCBI
This variant has been obsoleted and is no longer valid.