esv3787211
- 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:71,950
- Description:Chr8:g.115948641_115876692ins
- 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: 342 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 342 SVs from 50 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3787211 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 114,864,463 | 114,936,412 |
| esv3787211 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 115,876,692 | 115,948,641 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16613855 | insertion | 1745779 | Curated | Curated | 24 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16613855 | Remapped | Perfect | NC_000008.11:g.114 864463_114936412in s? | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 114,864,463 | 114,936,412 |
| essv16613855 | Submitted genomic | NC_000008.10:g.115 876692_115948641in s? | GRCh37 (hg19) | NC_000008.10 | Chr8 | 115,876,692 | 115,948,641 |