esv3811103
- 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:106,326,459
- Description:Chr7:g.14277383_120204270ins
- 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: 272266 SVs from 152 studies. See in: genome view
Overlapping variant regions from other studies: 270770 SVs from 152 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3811103 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 14,237,758 | 120,564,216 |
| esv3811103 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 14,277,383 | 120,204,270 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16640501 | insertion | 2197588 | Curated | Curated | 23 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16640501 | Remapped | Good | NC_000007.14:g.142 37758_120564216ins ? | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 14,237,758 | 120,564,216 |
| essv16640501 | Submitted genomic | NC_000007.13:g.142 77383_120204270ins ? | GRCh37 (hg19) | NC_000007.13 | Chr7 | 14,277,383 | 120,204,270 |