esv998439
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:20,008
- 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: 4092 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 3802 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 1843 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv998439 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 21,173,442 | 21,193,449 |
| esv998439 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 21,378,771 | 21,398,778 |
| esv998439 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 19,643,430 | 19,663,437 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586710 | Remapped | Perfect | NC_000015.10:g.(?_ 21173442)_(2119344 9_?)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 21,173,442 | 21,193,449 |
| essv3586710 | Remapped | Perfect | NC_000015.9:g.(?_2 1378771)_(21398778 _?)del | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 21,378,771 | 21,398,778 |
| essv3586710 | Submitted genomic | NC_000015.8:g.(?_1 9643430)_(19663437 _?)del | NCBI36 (hg18) | NC_000015.8 | Chr15 | 19,643,430 | 19,663,437 |