nsv4450412
- 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:10,070,678
- Description:GRCh37/hg19 1q23.1-24.2(chr1:157321299-167391423)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: 23699 SVs from 128 studies. See in: genome view
Overlapping variant regions from other studies: 23699 SVs from 128 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4450412 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 157,351,509 | 167,422,186 |
| nsv4450412 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 157,321,299 | 167,391,423 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15777243 | copy number loss | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV000848773.2, VCV000688082.2 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15777243 | Remapped | Good | NC_000001.11:g.(?_ 157351509)_(167422 186_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 157,351,509 | 167,422,186 |
| nssv15777243 | Submitted genomic | NC_000001.10:g.(?_ 157321299)_(167391 423_?)del | GRCh37 (hg19) | NC_000001.10 | Chr1 | 157,321,299 | 167,391,423 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15777243 | GRCh37: NC_000001.10:g.(?_157321299)_(167391423_?)del | copy number loss | unknown | not provided | Pathogenic | ClinVar | RCV000848773.2, VCV000688082.2 | 1 |