esv3815576
- 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:412,897
- Description:Chr18:g.69404067_68991171ins
- 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: 1791 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 1791 SVs from 76 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3815576 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 71,323,935 | 71,736,831 |
| esv3815576 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000018.9 | Chr18 | 68,991,171 | 69,404,067 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16645497 | insertion | 1745787 | Curated | Curated | 15 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16645497 | Remapped | Perfect | NC_000018.10:g.713 23935_71736831ins? | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 71,323,935 | 71,736,831 |
| essv16645497 | Submitted genomic | NC_000018.9:g.6899 1171_69404067ins? | GRCh37 (hg19) | NC_000018.9 | Chr18 | 68,991,171 | 69,404,067 |