esv3769495
- 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:30,453,350
- Description:Chr1:g.107914819_77384533ins
- 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: 72603 SVs from 142 studies. See in: genome view
Overlapping variant regions from other studies: 72504 SVs from 142 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3769495 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 76,918,848 | 107,372,197 |
| esv3769495 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 77,384,533 | 107,914,819 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16594127 | insertion | 1745780 | Curated | Curated | 25 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16594127 | Remapped | Good | NC_000001.11:g.769 18848_107372197ins ? | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 76,918,848 | 107,372,197 |
| essv16594127 | Submitted genomic | NC_000001.10:g.773 84533_107914819ins ? | GRCh37 (hg19) | NC_000001.10 | Chr1 | 77,384,533 | 107,914,819 |