nsv6314186
- 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:328,023
- Description:GRCh37/hg19 12p13.31(chr12:6872634-7244086) AND not specified
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1158 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 1124 SVs from 80 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6314186 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 6,763,468 | 7,091,490 |
| nsv6314186 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 6,872,634 | 7,244,086 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv17969505 | copy number gain | Multiple | Multiple | not specified | Uncertain significance | ClinVar | RCV002052969.3, VCV001527683.3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17969505 | Remapped | Pass | NC_000012.12:g.(?_ 6763468)_(7091490_ ?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 6,763,468 | 7,091,490 |
| nssv17969505 | Submitted genomic | NC_000012.11:g.(?_ 6872634)_(7244086_ ?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 6,872,634 | 7,244,086 |
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 |
|---|---|---|---|---|---|---|---|
| nssv17969505 | GRCh37: NC_000012.11:g.(?_6872634)_(7244086_?)dup | copy number gain | germline | not specified | Uncertain significance | ClinVar | RCV002052969.3, VCV001527683.3 |