esv3765456
- 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:67
- Description:Chr12:g.72863914_72863848ins
- 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: 105 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 105 SVs from 27 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3765456 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 72,470,068 | 72,470,134 |
| esv3765456 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 72,863,848 | 72,863,914 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16589636 | insertion | 1745789 | Curated | Curated | 7 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16589636 | Remapped | Perfect | NC_000012.12:g.724 70068_72470134ins? | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 72,470,068 | 72,470,134 |
| essv16589636 | Submitted genomic | NC_000012.11:g.728 63848_72863914ins? | GRCh37 (hg19) | NC_000012.11 | Chr12 | 72,863,848 | 72,863,914 |