esv3774835
- 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:4,991
- Description:Chr17:g.40432731_40427741ins
- 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: 74 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 72 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3774835 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 42,275,723 | 42,280,713 |
| esv3774835 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 40,427,741 | 40,432,731 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16600197 | insertion | 1745788 | Curated | Curated | 14 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16600197 | Remapped | Perfect | NC_000017.11:g.422 75723_42280713ins? | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 42,275,723 | 42,280,713 |
| essv16600197 | Submitted genomic | NC_000017.10:g.404 27741_40432731ins? | GRCh37 (hg19) | NC_000017.10 | Chr17 | 40,427,741 | 40,432,731 |