esv3789162
- 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:645
- Description:Chr9:g.127560620_127559976ins
- 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: 90 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 90 SVs from 19 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3789162 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 124,797,697 | 124,798,341 |
| esv3789162 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 127,559,976 | 127,560,620 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16615996 | insertion | 1745779 | Curated | Curated | 24 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16615996 | Remapped | Perfect | NC_000009.12:g.124 797697_124798341in s? | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 124,797,697 | 124,798,341 |
| essv16615996 | Submitted genomic | NC_000009.11:g.127 559976_127560620in s? | GRCh37 (hg19) | NC_000009.11 | Chr9 | 127,559,976 | 127,560,620 |