nsv3893968
- 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:2,667,227
- Description:GRCh37/hg19 11p13-12(chr11:34189942-36857171) AND not specified
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 6402 SVs from 112 studies. See in: genome view
Overlapping variant regions from other studies: 6407 SVs from 112 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3893968 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 34,168,395 | 36,835,621 |
| nsv3893968 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 34,189,942 | 36,857,171 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv17969458 | copy number gain | Multiple | Multiple | not specified | Uncertain significance | ClinVar | RCV002052922.3, VCV001527636.3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17969458 | Remapped | Perfect | NC_000011.10:g.(?_ 34168395)_(3683562 1_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 34,168,395 | 36,835,621 |
| nssv17969458 | Submitted genomic | NC_000011.9:g.(?_3 4189942)_(36857171 _?)dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 34,189,942 | 36,857,171 |
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 |
|---|---|---|---|---|---|---|---|
| nssv17969458 | GRCh37: NC_000011.9:g.(?_34189942)_(36857171_?)dup | copy number gain | germline | not specified | Uncertain significance | ClinVar | RCV002052922.3, VCV001527636.3 |