esv1003105
- 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:46,701
- 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: 315 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 315 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 82 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1003105 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 82,773,042 | 82,819,742 |
| esv1003105 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 83,166,821 | 83,213,521 |
| esv1003105 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 81,690,952 | 81,737,652 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3565042 | Remapped | Perfect | NC_000012.12:g.(82 773042_?)_(?_82819 742)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 82,773,042 | 82,819,742 |
| essv3565042 | Remapped | Perfect | NC_000012.11:g.(83 166821_?)_(?_83213 521)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 83,166,821 | 83,213,521 |
| essv3565042 | Submitted genomic | NC_000012.10:g.(81 690952_?)_(?_81737 652)del45850 | NCBI36 (hg18) | NC_000012.10 | Chr12 | 81,690,952 | 81,737,652 |