nsv4674784
- 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:3,006,809
- Description:GRCh37/hg19 2p25.3(chr2:1045542-4104255)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: 14265 SVs from 112 studies. See in: genome view
Overlapping variant regions from other studies: 14273 SVs from 112 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4674784 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 1,049,856 | 4,056,664 |
| nsv4674784 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 1,045,542 | 4,104,255 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16206555 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV001005221.1, VCV000814209.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16206555 | Remapped | Good | NC_000002.12:g.(?_ 1049856)_(4056664_ ?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,049,856 | 4,056,664 |
| nssv16206555 | Submitted genomic | NC_000002.11:g.(?_ 1045542)_(4104255_ ?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,045,542 | 4,104,255 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16206555 | GRCh37: NC_000002.11:g.(?_1045542)_(4104255_?)dup | copy number gain | germline | not provided | Uncertain significance | ClinVar | RCV001005221.1, VCV000814209.1 | 3 |