esv1001162
- 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:25,731
- 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: 699 SVs from 62 studies. See in: genome view
Overlapping variant regions from other studies: 754 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 548 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 | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1001162 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 19,170,619 | 19,196,349 |
| esv1001162 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 19,791,357 | 19,817,087 |
| esv1001162 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000014.7 | Chr14 | 18,861,357 | 18,887,087 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586085 | Remapped | Perfect | NC_000014.9:g.(?_1 9170619)_(19196349 _?)del | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 19,170,619 | 19,196,349 |
| essv3586085 | Remapped | Perfect | NC_000014.8:g.(?_1 9791357)_(19817087 _?)del | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 19,791,357 | 19,817,087 |
| essv3586085 | Submitted genomic | NC_000014.7:g.(?_1 8861357)_(18887087 _?)del | NCBI36 (hg18) | NC_000014.7 | Chr14 | 18,861,357 | 18,887,087 |