esv1000794
- 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:17,731
- 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: 557 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 557 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 373 SVs from 23 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1000794 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 107,360,721 | 107,378,451 |
| esv1000794 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 107,231,447 | 107,249,177 |
| esv1000794 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 106,736,657 | 106,754,387 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564879 | Remapped | Perfect | NC_000011.10:g.(10 7360721_?)_(?_1073 78451)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 107,360,721 | 107,378,451 |
| essv3564879 | Remapped | Perfect | NC_000011.9:g.(107 231447_?)_(?_10724 9177)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 107,231,447 | 107,249,177 |
| essv3564879 | Submitted genomic | NC_000011.8:g.(106 736657_?)_(?_10675 4387)del12402 | NCBI36 (hg18) | NC_000011.8 | Chr11 | 106,736,657 | 106,754,387 |