esv3804328
- 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:
Chr4:g.o(81910059_81912059)_chr3:(57415685_57417685)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: 56 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 142 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 56 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 142 SVs from 31 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| esv3804328 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 57,429,958 | 57,431,958 | 57,429,958 | 57,431,958 | |
| esv3804328 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 80,988,905 | 80,990,905 | 80,988,905 | 80,990,905 | - |
| esv3804328 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 57,415,685 | 57,417,685 | 57,415,685 | 57,417,685 | |||
| esv3804328 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 81,910,059 | 81,912,059 | 81,910,059 | 81,912,059 | - |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16632916 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv16632916 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 57,429,958 | 57,431,958 | 57,429,958 | 57,431,958 | not reported |
| essv16632916 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 80,988,905 | 80,990,905 | 80,988,905 | 80,990,905 | - |
| essv16632916 | Submitted genomic | GRCh37 (hg19) | NC_000003.11 | Chr3 | 57,415,685 | 57,417,685 | 57,415,685 | 57,417,685 | not reported | ||
| essv16632916 | Submitted genomic | GRCh37 (hg19) | NC_000004.11 | Chr4 | 81,910,059 | 81,912,059 | 81,910,059 | 81,912,059 | - |