esv3793068
- 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:91,276,834
- Description:Chr10:g.18775843_111523505ins
- Publication(s):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: 230023 SVs from 146 studies. See in: genome view
Overlapping variant regions from other studies: 227957 SVs from 146 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3793068 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 18,486,914 | 109,763,747 |
| esv3793068 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 18,775,843 | 111,523,505 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16620418 | insertion | 2197585 | Curated | Curated | 78 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16620418 | Remapped | Good | NC_000010.11:g.184 86914_109763747ins ? | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 18,486,914 | 109,763,747 |
| essv16620418 | Submitted genomic | NC_000010.10:g.187 75843_111523505ins ? | GRCh37 (hg19) | NC_000010.10 | Chr10 | 18,775,843 | 111,523,505 |