esv1842975
- Organism: Homo sapiens
- Study:estd188 (Pinto et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:357,988
- Publication(s):Pinto et al. 2011
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: 1296 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1301 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 492 SVs from 25 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1842975 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 53,618,908 | 53,976,895 |
| esv1842975 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 55,378,668 | 55,736,655 |
| esv1842975 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 55,048,674 | 55,406,661 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4403162 | Remapped | Perfect | NC_000010.11:g.(?_ 53618908)_(5397689 5_?)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 53,618,908 | 53,976,895 |
| essv4403162 | Remapped | Perfect | NC_000010.10:g.(?_ 55378668)_(5573665 5_?)del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 55,378,668 | 55,736,655 |
| essv4403162 | Submitted genomic | NC_000010.9:g.(?_5 5048674)_(55406661 _?)del | NCBI36 (hg18) | NC_000010.9 | Chr10 | 55,048,674 | 55,406,661 |