nsv4728461
- 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:797,870
- Description:GRCh37/hg19 1p36.32(chr1:3202162-4143527)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: 3711 SVs from 103 studies. See in: genome view
Overlapping variant regions from other studies: 3707 SVs from 103 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4728461 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 3,285,598 | 4,083,467 |
| nsv4728461 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 3,202,162 | 4,143,527 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16254636 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV001260108.1, VCV000980932.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16254636 | Remapped | Pass | NC_000001.11:g.(?_ 3285598)_(4083467_ ?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 3,285,598 | 4,083,467 |
| nssv16254636 | Submitted genomic | NC_000001.10:g.(?_ 3202162)_(4143527_ ?)dup | GRCh37 (hg19) | NC_000001.10 | Chr1 | 3,202,162 | 4,143,527 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16254636 | GRCh37: NC_000001.10:g.(?_3202162)_(4143527_?)dup | copy number gain | germline | not provided | Uncertain significance | ClinVar | RCV001260108.1, VCV000980932.1 | 3 |