esv999428
- 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:38,298
- 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: 289 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 346 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 145 SVs from 19 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv999428 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 149,193,530 | 149,231,827 |
| esv999428 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 144,672,443 | 144,710,724 |
| esv999428 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 143,383,800 | 143,422,081 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586330 | Remapped | Good | NC_000001.11:g.(?_ 149193530)_(149231 827_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 149,193,530 | 149,231,827 |
| essv3586330 | Remapped | Perfect | NC_000001.10:g.(?_ 144672443)_(144710 724_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 144,672,443 | 144,710,724 |
| essv3586330 | Submitted genomic | NC_000001.9:g.(?_1 43383800)_(1434220 81_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 143,383,800 | 143,422,081 |