esv3995697
- Organism: Homo sapiens
- Study:estd218 (Simpson et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:102,480
- Publication(s):Simpson et al. 2015
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: 475 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 475 SVs from 65 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3995697 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 44,350,987 | 44,453,466 |
| esv3995697 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 44,820,190 | 44,922,669 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Subject Phenotype | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|---|
| essv26047223 | copy number gain | SLI_80_2 | SNP array | Probe signal intensity | Specific language impairment 1 | 3 | 17 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv26047223 | Remapped | Perfect | NC_000014.9:g.(?_4 4350987)_(44453466 _?)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 44,350,987 | 44,453,466 |
| essv26047223 | Submitted genomic | NC_000014.8:g.(?_4 4820190)_(44922669 _?)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 44,820,190 | 44,922,669 |