nsv4674161
- 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:23,250,807
- Description:GRCh37/hg19 5p15.33-14.2(chr5:113576-23364376)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: 80872 SVs from 141 studies. See in: genome view
Overlapping variant regions from other studies: 80902 SVs from 141 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4674161 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 113,461 | 23,364,267 |
| nsv4674161 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000005.9 | Chr5 | 113,576 | 23,364,376 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16208007 | copy number loss | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV001005642.1, VCV000814652.1 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16208007 | Remapped | Perfect | NC_000005.10:g.(?_ 113461)_(23364267_ ?)del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 113,461 | 23,364,267 |
| nssv16208007 | Submitted genomic | NC_000005.9:g.(?_1 13576)_(23364376_? )del | GRCh37 (hg19) | NC_000005.9 | Chr5 | 113,576 | 23,364,376 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16208007 | GRCh37: NC_000005.9:g.(?_113576)_(23364376_?)del | copy number loss | germline | not provided | Pathogenic | ClinVar | RCV001005642.1, VCV000814652.1 | 1 |