nsv4456509
- 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:419,813
- Description:GRCh37/hg19 9q34.3(chr9:139766260-140186072)x3 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: 2401 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 2401 SVs from 95 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4456509 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 136,871,808 | 137,291,620 |
| nsv4456509 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 139,766,260 | 140,186,072 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15772964 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV000848688.2, VCV000687997.2 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15772964 | Remapped | Perfect | NC_000009.12:g.(?_ 136871808)_(137291 620_?)dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 136,871,808 | 137,291,620 |
| nssv15772964 | Submitted genomic | NC_000009.11:g.(?_ 139766260)_(140186 072_?)dup | GRCh37 (hg19) | NC_000009.11 | Chr9 | 139,766,260 | 140,186,072 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15772964 | GRCh37: NC_000009.11:g.(?_139766260)_(140186072_?)dup | copy number gain | unknown | not provided | Uncertain significance | ClinVar | RCV000848688.2, VCV000687997.2 | 3 |