esv3762702
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:copy number variation
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:617,034
- Description:Chr4:g.33100162_33717193del
- Publication(s):Campbell et al. 2010, Forbes et al. 2008, Forbes et al. 2008
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: 1604 SVs from 82 studies. See in: genome view
Overlapping variant regions from other studies: 1604 SVs from 82 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3762702 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 33,098,539 | 33,715,572 |
| esv3762702 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 33,100,161 | 33,717,194 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16586663 | deletion | 1109530 | Curated | Curated | 54 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16586663 | Remapped | Perfect | NC_000004.12:g.330 98539_33715572del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 33,098,539 | 33,715,572 |
| essv16586663 | Submitted genomic | NC_000004.11:g.331 00161_33717194del | GRCh37 (hg19) | NC_000004.11 | Chr4 | 33,100,161 | 33,717,194 |