esv990020
- 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:24,510
- 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: 366 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 366 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 140 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv990020 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 1,892,921 | 1,917,430 |
| esv990020 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 1,914,151 | 1,938,660 |
| esv990020 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 1,870,727 | 1,895,236 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564280 | Remapped | Perfect | NC_000011.10:g.(18 92921_?)_(?_191743 0)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 1,892,921 | 1,917,430 |
| essv3564280 | Remapped | Perfect | NC_000011.9:g.(191 4151_?)_(?_1938660 )del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 1,914,151 | 1,938,660 |
| essv3564280 | Submitted genomic | NC_000011.8:g.(187 0727_?)_(?_1895236 )del22296 | NCBI36 (hg18) | NC_000011.8 | Chr11 | 1,870,727 | 1,895,236 |