esv995112
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:34,286
- Publication(s):Pang et al. 2010
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: 1005 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 1005 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 645 SVs from 29 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv995112 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 1,579,598 | 1,613,883 |
| esv995112 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 1,560,244 | 1,594,529 |
| esv995112 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000020.9 | Chr20 | 1,508,244 | 1,542,529 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3565751 | Remapped | Perfect | NC_000020.11:g.(15 79598_?)_(?_161388 3)del | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 1,579,598 | 1,613,883 |
| essv3565751 | Remapped | Perfect | NC_000020.10:g.(15 60244_?)_(?_159452 9)del | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 1,560,244 | 1,594,529 |
| essv3565751 | Submitted genomic | NC_000020.9:g.(150 8244_?)_(?_1542529 )del32792 | NCBI36 (hg18) | NC_000020.9 | Chr20 | 1,508,244 | 1,542,529 |