nsv4728604
- 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:3,953,469
- Description:GRCh37/hg19 3q27.1-27.3(chr3:182877291-186830759)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: 11753 SVs from 116 studies. See in: genome view
Overlapping variant regions from other studies: 11754 SVs from 116 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4728604 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 183,159,503 | 187,112,971 |
| nsv4728604 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 182,877,291 | 186,830,759 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16255537 | copy number loss | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV001259730.1, VCV000980554.1 | 1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16255537 | Remapped | Perfect | NC_000003.12:g.(?_ 183159503)_(187112 971_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 183,159,503 | 187,112,971 |
| nssv16255537 | Submitted genomic | NC_000003.11:g.(?_ 182877291)_(186830 759_?)del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 182,877,291 | 186,830,759 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16255537 | GRCh37: NC_000003.11:g.(?_182877291)_(186830759_?)del | copy number loss | germline | not provided | Pathogenic | ClinVar | RCV001259730.1, VCV000980554.1 | 1 |