nsv7097331
- 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:1,991,842
- Description:NC_000006.11:g.(?_42162409)_(44154249_?)del 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: 5393 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 5393 SVs from 96 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 |
---|---|---|---|---|---|---|---|---|---|
nsv7097331 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 42,194,671 | 44,186,512 |
nsv7097331 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 42,162,409 | 44,154,249 |
Variant Call Information
Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
---|---|---|---|---|---|---|---|
nssv18792091 | deletion | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV003107587.2, VCV002424354.3 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18792091 | Remapped | Perfect | NC_000006.12:g.(?_ 42194671)_(4418651 2_?)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 42,194,671 | 44,186,512 |
nssv18792091 | Submitted genomic | NC_000006.11:g.(?_ 42162409)_(4415424 9_?)del | GRCh37 (hg19) | NC_000006.11 | Chr6 | 42,162,409 | 44,154,249 |
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 |
---|---|---|---|---|---|---|---|
nssv18792091 | GRCh37: NC_000006.11:g.(?_42162409)_(44154249_?)del | deletion | germline | not provided | Uncertain significance | ClinVar | RCV003107587.2, VCV002424354.3 |