nsv1067758 - (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:12
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:2,811,999
- 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: nsv3910011
- ClinVar: SCV000190727
- ClinVar: SCV000190729
- ClinVar: SCV000190730
- ClinVar: SCV000190731
- HP: 0000047
- HP: 0000077
- HP: 0000175
- HP: 0000204
- HP: 0001249
- HP: 0001263
- HP: 0001627
- HP: 0001629
- HP: 0001684
- HP: 0002116
- HP: 0004322
- dbVar: nssv15139527
- dbVar: nssv15139690
- dbVar: nsv4351322
- Overlapping Genes
Source: NCBI
This variant has been obsoleted and is no longer valid.