nsv4729273
- 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:691,451
- Description:GRCh37/hg19 6q22.1(chr6:117190128-117881578)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: 1620 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 1620 SVs from 76 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4729273 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 116,868,965 | 117,560,415 |
| nsv4729273 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 117,190,128 | 117,881,578 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16254324 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV001259398.1, VCV000980222.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16254324 | Remapped | Perfect | NC_000006.12:g.(?_ 116868965)_(117560 415_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 116,868,965 | 117,560,415 |
| nssv16254324 | Submitted genomic | NC_000006.11:g.(?_ 117190128)_(117881 578_?)dup | GRCh37 (hg19) | NC_000006.11 | Chr6 | 117,190,128 | 117,881,578 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16254324 | GRCh37: NC_000006.11:g.(?_117190128)_(117881578_?)dup | copy number gain | germline | not provided | Uncertain significance | ClinVar | RCV001259398.1, VCV000980222.1 | 3 |