esv3791864
- 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:508,387
- Description:Chr5:g.57918535_58426921ins
- 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: 1314 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 1314 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3791864 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 58,622,708 | 59,131,094 |
| esv3791864 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000005.9 | Chr5 | 57,918,535 | 58,426,921 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16618995 | insertion | 2197585 | Curated | Curated | 78 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16618995 | Remapped | Perfect | NC_000005.10:g.586 22708_59131094ins? | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 58,622,708 | 59,131,094 |
| essv16618995 | Submitted genomic | NC_000005.9:g.5791 8535_58426921ins? | GRCh37 (hg19) | NC_000005.9 | Chr5 | 57,918,535 | 58,426,921 |