nsv6638032
- 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:186,505
- Description:GRCh37/hg19 9q22.31(chr9:95076710-95263214)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: 485 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 485 SVs from 51 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6638032 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 92,314,428 | 92,500,932 |
| nsv6638032 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 95,076,710 | 95,263,214 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18330841 | copy number loss | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV002472702.1, VCV001807896.1 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18330841 | Remapped | Perfect | NC_000009.12:g.(?_ 92314428)_(9250093 2_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 92,314,428 | 92,500,932 |
| nssv18330841 | Submitted genomic | NC_000009.11:g.(?_ 95076710)_(9526321 4_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 95,076,710 | 95,263,214 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv18330841 | GRCh37: NC_000009.11:g.(?_95076710)_(95263214_?)del | copy number loss | unknown | not provided | Uncertain significance | ClinVar | RCV002472702.1, VCV001807896.1 | 1 |