nsv4674695
- 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:2,444,346
- Description:GRCh37/hg19 4q13.2(chr4:67392949-69837294)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: 8333 SVs from 123 studies. See in: genome view
Overlapping variant regions from other studies: 8333 SVs from 123 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4674695 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 66,527,231 | 68,971,576 |
| nsv4674695 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 67,392,949 | 69,837,294 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16206707 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV001005552.1, VCV000814562.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16206707 | Remapped | Perfect | NC_000004.12:g.(?_ 66527231)_(6897157 6_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 66,527,231 | 68,971,576 |
| nssv16206707 | Submitted genomic | NC_000004.11:g.(?_ 67392949)_(6983729 4_?)dup | GRCh37 (hg19) | NC_000004.11 | Chr4 | 67,392,949 | 69,837,294 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16206707 | GRCh37: NC_000004.11:g.(?_67392949)_(69837294_?)dup | copy number gain | germline | not provided | Uncertain significance | ClinVar | RCV001005552.1, VCV000814562.1 | 3 |