nsv7097922
- 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:161
- Description:NC_000009.11:g.(?_116037910)_(116038070_?)dup 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: 51 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 51 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv7097922 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 113,275,630 | 113,275,790 |
| nsv7097922 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 116,037,910 | 116,038,070 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv18789916 | duplication | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV003113569.1, VCV002425200.2 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18789916 | Remapped | Perfect | NC_000009.12:g.(?_ 113275630)_(113275 790_?)dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 113,275,630 | 113,275,790 |
| nssv18789916 | Submitted genomic | NC_000009.11:g.(?_ 116037910)_(116038 070_?)dup | GRCh37 (hg19) | NC_000009.11 | Chr9 | 116,037,910 | 116,038,070 |
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 |
|---|---|---|---|---|---|---|---|
| nssv18789916 | GRCh37: NC_000009.11:g.(?_116037910)_(116038070_?)dup | duplication | germline | not provided | Uncertain significance | ClinVar | RCV003113569.1, VCV002425200.2 |