nsv6637694
- 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:1,061,707
- Description:GRCh37/hg19 22q11.1-11.21(chr22:16888900-17948922)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: 3628 SVs from 102 studies. See in: genome view
Overlapping variant regions from other studies: 3660 SVs from 104 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6637694 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 16,408,174 | 17,469,880 |
| nsv6637694 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000022.10 | Chr22 | 16,888,900 | 17,948,922 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18330134 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV002473866.1, VCV001808549.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18330134 | Remapped | Good | NC_000022.11:g.(?_ 16408174)_(1746988 0_?)dup | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 16,408,174 | 17,469,880 |
| nssv18330134 | Submitted genomic | NC_000022.10:g.(?_ 16888900)_(1794892 2_?)dup | GRCh37 (hg19) | NC_000022.10 | Chr22 | 16,888,900 | 17,948,922 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv18330134 | GRCh37: NC_000022.10:g.(?_16888900)_(17948922_?)dup | copy number gain | unknown | not provided | Uncertain significance | ClinVar | RCV002473866.1, VCV001808549.1 | 3 |