esv3766819
- 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:87,613,574
- Description:Chr2:g.46042537_134186542ins
- 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: 208236 SVs from 151 studies. See in: genome view
Overlapping variant regions from other studies: 207577 SVs from 151 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3766819 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 45,815,398 | 133,428,971 |
| esv3766819 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 46,042,537 | 134,186,542 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16591151 | insertion | 2197587 | Curated | Curated | 43 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16591151 | Remapped | Good | NC_000002.12:g.458 15398_133428971ins ? | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 45,815,398 | 133,428,971 |
| essv16591151 | Submitted genomic | NC_000002.11:g.460 42537_134186542ins ? | GRCh37 (hg19) | NC_000002.11 | Chr2 | 46,042,537 | 134,186,542 |