nsv6637627
- 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:823,649
- Description:GRCh37/hg19 12p13.31(chr12:8781515-9605163)x4 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: 3182 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 3182 SVs from 97 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6637627 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 8,628,919 | 9,452,567 |
| nsv6637627 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 8,781,515 | 9,605,163 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18330916 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV002472777.1, VCV001807971.1 | 4 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18330916 | Remapped | Perfect | NC_000012.12:g.(?_ 8628919)_(9452567_ ?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 8,628,919 | 9,452,567 |
| nssv18330916 | Submitted genomic | NC_000012.11:g.(?_ 8781515)_(9605163_ ?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 8,781,515 | 9,605,163 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv18330916 | GRCh37: NC_000012.11:g.(?_8781515)_(9605163_?)dup | copy number gain | unknown | not provided | Uncertain significance | ClinVar | RCV002472777.1, VCV001807971.1 | 4 |