esv3808297
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:complex chromosomal rearrangement
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,001
- Description:
Chr12:g.(77408513_77410513)_chr3:o(32810270_32812270)bkpt - 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: 54 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 82 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 54 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 82 SVs from 26 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| esv3808297 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 32,768,778 | 32,770,778 | 32,768,778 | 32,770,778 | - |
| esv3808297 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 77,014,733 | 77,016,733 | 77,014,733 | 77,016,733 | |
| esv3808297 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 32,810,270 | 32,812,270 | 32,810,270 | 32,812,270 | - | ||
| esv3808297 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 77,408,513 | 77,410,513 | 77,408,513 | 77,410,513 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16637339 | interchromosomal translocation | 2120208 | Curated | Curated | 66 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv16637339 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 32,768,778 | 32,770,778 | 32,768,778 | 32,770,778 | - |
| essv16637339 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 77,014,733 | 77,016,733 | 77,014,733 | 77,016,733 | not reported |
| essv16637339 | Submitted genomic | GRCh37 (hg19) | NC_000003.11 | Chr3 | 32,810,270 | 32,812,270 | 32,810,270 | 32,812,270 | - | ||
| essv16637339 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 77,408,513 | 77,410,513 | 77,408,513 | 77,410,513 | not reported |