nsv4674036
- 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:5,408,189
- Description:GRCh37/hg19 2q37.2-37.3(chr2:236172348-241611309)x1 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: 16916 SVs from 119 studies. See in: genome view
Overlapping variant regions from other studies: 16849 SVs from 119 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4674036 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 235,263,704 | 240,671,892 |
| nsv4674036 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 236,172,348 | 241,611,309 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16208713 | copy number loss | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV001007525.1, VCV000816588.1 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16208713 | Remapped | Good | NC_000002.12:g.(?_ 235263704)_(240671 892_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 235,263,704 | 240,671,892 |
| nssv16208713 | Submitted genomic | NC_000002.11:g.(?_ 236172348)_(241611 309_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 236,172,348 | 241,611,309 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16208713 | GRCh37: NC_000002.11:g.(?_236172348)_(241611309_?)del | copy number loss | germline | not provided | Pathogenic | ClinVar | RCV001007525.1, VCV000816588.1 | 1 |