nsv4457587
- 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:2,369,760
- Description:GRCh37/hg19 17p13.2(chr17:3759126-6128911)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: 8770 SVs from 111 studies. See in: genome view
Overlapping variant regions from other studies: 8775 SVs from 111 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4457587 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 3,855,832 | 6,225,591 |
| nsv4457587 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 3,759,126 | 6,128,911 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15773443 | copy number loss | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV000849625.2, VCV000688934.2 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15773443 | Remapped | Good | NC_000017.11:g.(?_ 3855832)_(6225591_ ?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 3,855,832 | 6,225,591 |
| nssv15773443 | Submitted genomic | NC_000017.10:g.(?_ 3759126)_(6128911_ ?)del | GRCh37 (hg19) | NC_000017.10 | Chr17 | 3,759,126 | 6,128,911 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15773443 | GRCh37: NC_000017.10:g.(?_3759126)_(6128911_?)del | copy number loss | unknown | not provided | Uncertain significance | ClinVar | RCV000849625.2, VCV000688934.2 | 1 |