nsv984559
- Organism: Homo sapiens
- Study:nstd91 (Sallustio et al. 2014)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:42,157
- Publication(s):Sallustio et al. 2014
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 242 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 245 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 88 SVs from 17 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nsv984559 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 71,174,769 | 71,216,925 |
nsv984559 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 73,789,685 | 73,831,841 |
nsv984559 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 72,979,505 | 73,021,661 |
Variant Call Information
Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation |
---|---|---|---|---|---|---|
nssv3217178 | copy number gain | SNP array | SNP genotyping analysis | Glomerulonephritis, IGA | association | Submitter |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv3217178 | Remapped | Perfect | NC_000009.12:g.(71 174769_?)_(?_71216 925)dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 71,174,769 | 71,216,925 |
nssv3217178 | Remapped | Perfect | NC_000009.11:g.(73 789685_?)_(?_73831 841)dup | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 73,789,685 | 73,831,841 |
nssv3217178 | Submitted genomic | NC_000009.10:g.(72 979505_?)_(?_73021 661)dup | NCBI36 (hg18) | NC_000009.10 | Chr9 | 72,979,505 | 73,021,661 |
No validation data were submitted for this variant
Clinical Assertions
Variant Call ID | HGVS | Type | Subject Phenotype | Clinical Interpretation | Source of Interpretation |
---|---|---|---|---|---|
nssv3217178 | NCBI36: NC_000009.10:g.(72979505_?)_(?_73021661)dup | copy number gain | Glomerulonephritis, IGA | association | Submitter |