nsv4729095
- 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:731,869
- Description:GRCh37/hg19 15q15.1(chr15:40464942-41196807)x4 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: 2225 SVs from 87 studies. See in: genome view
Overlapping variant regions from other studies: 2225 SVs from 87 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4729095 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 40,172,741 | 40,904,609 |
| nsv4729095 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 40,464,942 | 41,196,807 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16254226 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV001259208.1, VCV000980032.1 | 4 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16254226 | Remapped | Perfect | NC_000015.10:g.(?_ 40172741)_(4090460 9_?)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 40,172,741 | 40,904,609 |
| nssv16254226 | Submitted genomic | NC_000015.9:g.(?_4 0464942)_(41196807 _?)dup | GRCh37 (hg19) | NC_000015.9 | Chr15 | 40,464,942 | 41,196,807 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16254226 | GRCh37: NC_000015.9:g.(?_40464942)_(41196807_?)dup | copy number gain | germline | not provided | Uncertain significance | ClinVar | RCV001259208.1, VCV000980032.1 | 4 |