esv3791002
- 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:756
- Description:Chr13:g.96884225_96884980ins
- 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: 203 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 203 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3791002 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 96,231,971 | 96,232,726 |
| esv3791002 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 96,884,225 | 96,884,980 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16618114 | insertion | 2197582 | Curated | Curated | 54 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16618114 | Remapped | Perfect | NC_000013.11:g.962 31971_96232726ins? | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 96,231,971 | 96,232,726 |
| essv16618114 | Submitted genomic | NC_000013.10:g.968 84225_96884980ins? | GRCh37 (hg19) | NC_000013.10 | Chr13 | 96,884,225 | 96,884,980 |