esv3807329
- 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:Chr10:g.(62183381_62185381)_chr12:(114998434_1
15000434)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: 58 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 87 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 58 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 87 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 | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv3807329 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 60,423,623 | 60,425,623 | 60,423,623 | 60,425,623 |
| esv3807329 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 114,560,629 | 114,562,629 | 114,560,629 | 114,562,629 |
| esv3807329 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 62,183,381 | 62,185,381 | 62,183,381 | 62,185,381 | ||
| esv3807329 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 114,998,434 | 115,000,434 | 114,998,434 | 115,000,434 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16636258 | interchromosomal translocation | 2120209 | Curated | Curated | 35 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv16636258 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 60,423,623 | 60,425,623 | 60,423,623 | 60,425,623 | not reported |
| essv16636258 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 114,560,629 | 114,562,629 | 114,560,629 | 114,562,629 | not reported |
| essv16636258 | Submitted genomic | GRCh37 (hg19) | NC_000010.10 | Chr10 | 62,183,381 | 62,185,381 | 62,183,381 | 62,185,381 | not reported | ||
| essv16636258 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 114,998,434 | 115,000,434 | 114,998,434 | 115,000,434 | not reported |