nsv6637687
- 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:7,935,022
- Description:GRCh37/hg19 11q22.1-22.3(chr11:101371503-109306519)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: 21611 SVs from 126 studies. See in: genome view
Overlapping variant regions from other studies: 21614 SVs from 126 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6637687 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 101,500,772 | 109,435,793 |
| nsv6637687 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 101,371,503 | 109,306,519 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18329560 | copy number loss | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV002472494.1, VCV001807688.1 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18329560 | Remapped | Perfect | NC_000011.10:g.(?_ 101500772)_(109435 793_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 101,500,772 | 109,435,793 |
| nssv18329560 | Submitted genomic | NC_000011.9:g.(?_1 01371503)_(1093065 19_?)del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 101,371,503 | 109,306,519 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv18329560 | GRCh37: NC_000011.9:g.(?_101371503)_(109306519_?)del | copy number loss | unknown | not provided | Pathogenic | ClinVar | RCV002472494.1, VCV001807688.1 | 1 |