esv3802092
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:insertion
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:51,377,222
- Description:Chr1:g.120067696_68613535ins
- Publication(s):Forbes et al. 2008, Forbes et al. 2008, Zhang et al. 2012
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: 121248 SVs from 143 studies. See in: genome view
Overlapping variant regions from other studies: 121157 SVs from 143 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3802092 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 68,147,852 | 119,525,073 |
| esv3802092 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 68,613,535 | 120,067,696 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16630424 | insertion | 1745787 | Curated | Curated | 15 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16630424 | Remapped | Good | NC_000001.11:g.681 47852_119525073ins ? | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 68,147,852 | 119,525,073 |
| essv16630424 | Submitted genomic | NC_000001.10:g.686 13535_120067696ins ? | GRCh37 (hg19) | NC_000001.10 | Chr1 | 68,613,535 | 120,067,696 |