nsv1067632 - (obsolete)
- Organism: Homo sapiens
- Study:nstd101 (obsolete - ClinGen Kaminsky et al. 2011)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:10
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:156,011,528
- Description: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):Kaminsky et al. 2011
- Replacement Description: Replaced nstd101 variant regions with variants in [nstd102|/dbvar/studies/nstd102]
- Replacement Variant: nsv3907094
- ClinVar: SCV000190791
- ClinVar: SCV000190792
- ClinVar: SCV000190794
- HP: 0000047
- HP: 0000152
- HP: 0000153
- HP: 0000238
- HP: 0000280
- HP: 0000365
- HP: 0000582
- HP: 0000717
- HP: 0000924
- HP: 0001172
- HP: 0001263
- HP: 0004209
- HP: 0004322
- HP: 0100259
- dbVar: nssv15161379
- dbVar: nssv15161580
- dbVar: nsv4352574
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.