nsv4674044
- 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:257,086
- Description:GRCh37/hg19 3p21.31(chr3:47970377-48227462)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: 937 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 937 SVs from 64 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4674044 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 47,928,887 | 48,185,972 |
| nsv4674044 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 47,970,377 | 48,227,462 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16206646 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV001005431.1, VCV000814441.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16206646 | Remapped | Perfect | NC_000003.12:g.(?_ 47928887)_(4818597 2_?)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 47,928,887 | 48,185,972 |
| nssv16206646 | Submitted genomic | NC_000003.11:g.(?_ 47970377)_(4822746 2_?)dup | GRCh37 (hg19) | NC_000003.11 | Chr3 | 47,970,377 | 48,227,462 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16206646 | GRCh37: NC_000003.11:g.(?_47970377)_(48227462_?)dup | copy number gain | germline | not provided | Uncertain significance | ClinVar | RCV001005431.1, VCV000814441.1 | 3 |