nsv3874490
- 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:4,446
- Description:NC_000022.10:g.[30057723_30063344del;30063345_
30067790del] AND Neurofibromatosis, type 2 - Publication(s):ACMG Board of Directors et al. 2014, Evans et al. 1998, Green et al. 2013, Kalia et al. 2016, Miller et al. 2021, Miller et al. 2022, Radtke et al. 2020
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 82 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 82 SVs from 22 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|
| nsv3874490 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000022.11 | Chr22 | 29,667,356 | 29,671,801 |
| nsv3874490 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000022.10 | Chr22 | 30,063,345 | 30,067,790 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv15125278 | deletion | Multiple | Multiple | NEUROFIBROMATOSIS, TYPE II; NF2; Neurofibromatosis 2; Neurofibromatosis type 2; Neurofibromatosis, type 2 | Pathogenic | ClinVar | RCV000258245.2, VCV000267491.2 |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|
| nssv15125278 | Submitted genomic | NC_000022.11:g.296 67356_29671801del | GRCh38 (hg38) | NC_000022.11 | Chr22 | 29,667,356 | 29,671,801 |
| nssv15125278 | Submitted genomic | NC_000022.10:g.300 63345_30067790del | GRCh37 (hg19) | NC_000022.10 | Chr22 | 30,063,345 | 30,067,790 |
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 |
|---|---|---|---|---|---|---|---|
| nssv15125278 | GRCh37: NC_000022.10:g.30063345_30067790del, GRCh38: NC_000022.11:g.29667356_29671801del | deletion | somatic | NEUROFIBROMATOSIS, TYPE II; NF2; Neurofibromatosis 2; Neurofibromatosis type 2; Neurofibromatosis, type 2 | Pathogenic | ClinVar | RCV000258245.2, VCV000267491.2 |