nsv4729643
- 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:3,443,016
- Description:GRCh37/hg19 7q32.2-33(chr7:129605827-133093756)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: 8331 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 8293 SVs from 97 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4729643 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 129,965,987 | 133,409,002 |
| nsv4729643 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 129,605,827 | 133,093,756 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16254112 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV001258971.1, VCV000979795.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16254112 | Remapped | Good | NC_000007.14:g.(?_ 129965987)_(133409 002_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 129,965,987 | 133,409,002 |
| nssv16254112 | Submitted genomic | NC_000007.13:g.(?_ 129605827)_(133093 756_?)dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 129,605,827 | 133,093,756 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16254112 | GRCh37: NC_000007.13:g.(?_129605827)_(133093756_?)dup | copy number gain | germline | not provided | Uncertain significance | ClinVar | RCV001258971.1, VCV000979795.1 | 3 |