nsv6637234
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:340,797
- Description:GRCh37/hg19 11p15.4(chr11:5279153-5619949)x3 AND not provided
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1277 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 1277 SVs from 83 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6637234 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 5,257,923 | 5,598,719 |
| nsv6637234 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 5,279,153 | 5,619,949 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18329469 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV002472403.1, VCV001807597.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18329469 | Remapped | Perfect | NC_000011.10:g.(?_ 5257923)_(5598719_ ?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 5,257,923 | 5,598,719 |
| nssv18329469 | Submitted genomic | NC_000011.9:g.(?_5 279153)_(5619949_? )dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 5,279,153 | 5,619,949 |
No validation data were submitted for this variant
Clinical Assertions
| Variant Call ID | HGVS | Type | Allele Origin | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18329469 | GRCh37: NC_000011.9:g.(?_5279153)_(5619949_?)dup | copy number gain | unknown | not provided | Uncertain significance | ClinVar | RCV002472403.1, VCV001807597.1 | 3 |