nsv3890986
- 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:110,005
- Description:GRCh37/hg19 17q25.1(chr17:73517536-73627539)x1 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: 597 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 597 SVs from 70 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 |
---|---|---|---|---|---|---|---|---|---|
nsv3890986 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 75,521,455 | 75,631,459 |
nsv3890986 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 73,517,536 | 73,627,539 |
Variant Call Information
Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
---|---|---|---|---|---|---|---|---|
nssv15173479 | copy number loss | Multiple | Multiple | not provided | Benign | ClinVar | RCV000752191.2, VCV000615555.2 | 1 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15173479 | Remapped | Good | NC_000017.11:g.(?_ 75521455)_(7563145 9_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 75,521,455 | 75,631,459 |
nssv15173479 | Submitted genomic | NC_000017.10:g.(?_ 73517536)_(7362753 9_?)del | GRCh37 (hg19) | NC_000017.10 | Chr17 | 73,517,536 | 73,627,539 |
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 |
---|---|---|---|---|---|---|---|---|
nssv15173479 | GRCh37: NC_000017.10:g.(?_73517536)_(73627539_?)del | copy number loss | unknown | not provided | Benign | ClinVar | RCV000752191.2, VCV000615555.2 | 1 |