nsv6311440
- 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:29,386
- Description:NC_000003.11:g.(?_138091726)_(138121111_?)dup 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: 150 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 150 SVs from 28 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6311440 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 138,372,884 | 138,402,269 |
| nsv6311440 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 138,091,726 | 138,121,111 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv17968830 | duplication | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV001943027.1, VCV001411717.1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17968830 | Remapped | Perfect | NC_000003.12:g.(?_ 138372884)_(138402 269_?)dup | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 138,372,884 | 138,402,269 |
| nssv17968830 | Submitted genomic | NC_000003.11:g.(?_ 138091726)_(138121 111_?)dup | GRCh37 (hg19) | NC_000003.11 | Chr3 | 138,091,726 | 138,121,111 |
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 |
|---|---|---|---|---|---|---|---|
| nssv17968830 | GRCh37: NC_000003.11:g.(?_138091726)_(138121111_?)dup | duplication | germline | not provided | Uncertain significance | ClinVar | RCV001943027.1, VCV001411717.1 |