nsv3881924
- 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:131,332
- Description:GRCh37/hg19 2q23.1(chr2:148859098-148990429)x1 AND See cases
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 417 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 417 SVs from 44 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3881924 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 148,101,529 | 148,232,860 |
| nsv3881924 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 148,859,098 | 148,990,429 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15142359 | copy number loss | Multiple | Multiple | See cases | Uncertain significance | ClinVar | RCV000511235.2, VCV000443495.2 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15142359 | Remapped | Perfect | NC_000002.12:g.(?_ 148101529)_(148232 860_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 148,101,529 | 148,232,860 |
| nssv15142359 | Submitted genomic | NC_000002.11:g.(?_ 148859098)_(148990 429_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 148,859,098 | 148,990,429 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15142359 | GRCh37: NC_000002.11:g.(?_148859098)_(148990429_?)del | copy number loss | biparental | See cases | Uncertain significance | ClinVar | RCV000511235.2, VCV000443495.2 | 1 |