nsv3886007
- 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:290,674
- Description:GRCh37/hg19 6p21.33-21.32(chr6:31952482-32243155) AND not specified
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1627 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 1627 SVs from 85 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3886007 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 31,984,705 | 32,275,378 |
| nsv3886007 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 31,952,482 | 32,243,155 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv17970093 | copy number gain | Multiple | Multiple | not specified | Uncertain significance | ClinVar | RCV002053565.3, VCV001527233.3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17970093 | Remapped | Perfect | NC_000006.12:g.(?_ 31984705)_(3227537 8_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 31,984,705 | 32,275,378 |
| nssv17970093 | Submitted genomic | NC_000006.11:g.(?_ 31952482)_(3224315 5_?)dup | GRCh37 (hg19) | NC_000006.11 | Chr6 | 31,952,482 | 32,243,155 |
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 |
|---|---|---|---|---|---|---|---|
| nssv17970093 | GRCh37: NC_000006.11:g.(?_31952482)_(32243155_?)dup | copy number gain | germline | not specified | Uncertain significance | ClinVar | RCV002053565.3, VCV001527233.3 |