nsv7137135
- 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:6,205,824
- Description:GRCh37/hg19 14q31.3-32.13(chr14:88401076-94725706)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: 16223 SVs from 115 studies. See in: genome view
Overlapping variant regions from other studies: 16556 SVs from 115 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv7137135 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 87,934,732 | 94,140,555 |
| nsv7137135 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 88,401,076 | 94,725,706 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18830720 | copy number loss | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV003312295.1, VCV002570894.2 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18830720 | Remapped | Good | NC_000014.9:g.(?_8 7934732)_(94140555 _?)del | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 87,934,732 | 94,140,555 |
| nssv18830720 | Submitted genomic | NC_000014.8:g.(?_8 8401076)_(94725706 _?)del | GRCh37 (hg19) | NC_000014.8 | Chr14 | 88,401,076 | 94,725,706 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv18830720 | GRCh37: NC_000014.8:g.(?_88401076)_(94725706_?)del | copy number loss | germline | not provided | Pathogenic | ClinVar | RCV003312295.1, VCV002570894.2 | 1 |