nsv3877139
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:4,176,626
- Description:
NC_000001.11:g.(?_204033173)_(208209798_?)del AND Autism - Publication(s):Kushima et al. 2018, Miller et al. 2010, Shao et al. 2021
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 9336 SVs from 111 studies. See in: genome view
Overlapping variant regions from other studies: 9254 SVs from 111 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3877139 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000001.11 | Chr1 | 204,033,173 | 208,209,798 | ||
| nsv3877139 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 204,002,301 | 208,383,143 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv15145197 | deletion | Multiple | Multiple | AUTISM; Autism; Autistic Disorder; Autistic disorder of childhood onset | Likely pathogenic | ClinVar | RCV000754138.1, VCV000545154.1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15145197 | Submitted genomic | NC_000001.11:g.(?_ 204033173)_(208209 798_?)del | GRCh38 (hg38) | NC_000001.11 | Chr1 | 204,033,173 | 208,209,798 | ||
| nssv15145197 | Remapped | Good | NC_000001.10:g.(?_ 204002301)_(208383 143_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 204,002,301 | 208,383,143 |
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 |
|---|---|---|---|---|---|---|---|
| nssv15145197 | GRCh38: NC_000001.11:g.(?_204033173)_(208209798_?)del | deletion | germline | AUTISM; Autism; Autistic Disorder; Autistic disorder of childhood onset | Likely pathogenic | ClinVar | RCV000754138.1, VCV000545154.1 |