esv992072
- 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:22,740
- 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: 873 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 873 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 412 SVs from 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv992072 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 18,920,312 | 18,943,051 |
| esv992072 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 18,941,859 | 18,964,598 |
| esv992072 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 18,898,435 | 18,921,174 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586653 | Remapped | Perfect | NC_000011.10:g.(?_ 18920312)_(1894305 1_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 18,920,312 | 18,943,051 |
| essv3586653 | Remapped | Perfect | NC_000011.9:g.(?_1 8941859)_(18964598 _?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 18,941,859 | 18,964,598 |
| essv3586653 | Submitted genomic | NC_000011.8:g.(?_1 8898435)_(18921174 _?)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 18,898,435 | 18,921,174 |