nsv995204 - (obsolete)
- Organism: Homo sapiens
- Study:nstd37 (obsolete - ClinGen Laboratory-Submitted)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:9
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:90,669
- Description:See descriptions for individual calls in download files. PLEASE NOTE: The calls represented in this region now have equivalents in the study Clinical Structural Variants (nstd102). Please use the preferred nstd102 variant region accession for this variant; you can find it at top right under "Links to Other Resources" or in the mapping file provided here.
- Publication(s):Miller et al. 2010
- Replacement Description: Replaced nstd37 variant regions with variants in [nstd102|/dbvar/studies/nstd102]
- Replacement Variant: nsv3891513
- ClinVar: SCV000182619
- ClinVar: SCV000182620
- HP: 0000034
- HP: 0000098
- HP: 0000158
- HP: 0000212
- HP: 0000256
- HP: 0000280
- HP: 0000429
- HP: 0000729
- HP: 0000750
- HP: 0001007
- HP: 0001250
- HP: 0001252
- HP: 0001257
- HP: 0001263
- HP: 0001347
- HP: 0001371
- HP: 0001508
- HP: 0001548
- HP: 0002260
- HP: 0003307
- HP: 0004467
- HP: 0005753
- HP: 0200055
- dbVar: nssv15138619
- dbVar: nssv15138823
- dbVar: nsv4348560
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.