nsv4729763
- 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:633,107
- Description:GRCh37/hg19 17q11.2(chr17:27573641-28206747)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: 1991 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 1991 SVs from 77 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4729763 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 29,246,623 | 29,879,729 |
| nsv4729763 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 27,573,641 | 28,206,747 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16254294 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV001259333.1, VCV000980157.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16254294 | Remapped | Perfect | NC_000017.11:g.(?_ 29246623)_(2987972 9_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 29,246,623 | 29,879,729 |
| nssv16254294 | Submitted genomic | NC_000017.10:g.(?_ 27573641)_(2820674 7_?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 27,573,641 | 28,206,747 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16254294 | GRCh37: NC_000017.10:g.(?_27573641)_(28206747_?)dup | copy number gain | germline | not provided | Uncertain significance | ClinVar | RCV001259333.1, VCV000980157.1 | 3 |