nsv3883816
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37, GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:65,757
- Description:NC_000017.11:g.(?_61743007)_(61808763_?)del AND multiple conditions
- Publication(s):Alter et al. 2002, Berliner et al. 2007, Burstein et al. 2021, Miller et al. 2021, Miller et al. 2022, Moyer et al. 2014, Nelson et al. 2013, Nelson et al. 2019, No authors et al. 2014, No authors et al. 2021, No authors et al. 2021, Petrucelli et al. 1998, Scott et al. 2009, Stratton et al. 2008, Trepanier et al. 2004, US Preventive Services Task Force et al. 2019
- ClinVar: RCV000636238.2
- ClinVar: VCV000530388.2
- GeneReviews: NBK1247
- GeneReviews: NBK1401
- MONDO: 0012187
- MONDO: 0016419
- MedGen: C0346153
- MedGen: C1836860
- OMIM: 114480
- OMIM: 609054
- Orphanet: 84
- PubMed: 15604628
- PubMed: 17508274
- PubMed: 18163131
- PubMed: 20301425
- PubMed: 20301575
- PubMed: 20301753
- PubMed: 24366376
- PubMed: 24366402
- PubMed: 24432435
- PubMed: 26389210
- PubMed: 26389258
- PubMed: 31429903
- PubMed: 31479213
- PubMed: 34012068
- PubMed: 34242744
- PubMed: 35802134
- Overlapping Genes
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 284 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 284 SVs from 39 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nsv3883816 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000017.11 | Chr17 | 61,743,007 | 61,808,763 |
| nsv3883816 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 59,820,368 | 59,886,124 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv15153112 | deletion | Multiple | Multiple | BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer; BREAST CANCER; FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ; Familial cancer of breast; Fanconi Anemia; Fanconi anemia; Fanconi anemia, complementation group J | Pathogenic | ClinVar | RCV000636238.2, VCV000530388.2 |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nssv15153112 | Submitted genomic | NC_000017.11:g.(?_ 61743007)_(6180876 3_?)del | GRCh38 (hg38) | NC_000017.11 | Chr17 | 61,743,007 | 61,808,763 |
| nssv15153112 | Submitted genomic | NC_000017.10:g.(?_ 59820368)_(5988612 4_?)del | GRCh37 (hg19) | NC_000017.10 | Chr17 | 59,820,368 | 59,886,124 |
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 |
|---|---|---|---|---|---|---|---|
| nssv15153112 | GRCh37: NC_000017.10:g.(?_59820368)_(59886124_?)del, GRCh38: NC_000017.11:g.(?_61743007)_(61808763_?)del | deletion | germline | BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer; BREAST CANCER; FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ; Familial cancer of breast; Fanconi Anemia; Fanconi anemia; Fanconi anemia, complementation group J | Pathogenic | ClinVar | RCV000636238.2, VCV000530388.2 |