esv3809406
- 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.(31775635_31777635)_chr13:o(44163906_4
4165906)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: 99 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 171 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 99 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 171 SVs from 37 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| esv3809406 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 31,622,701 | 31,624,701 | 31,622,701 | 31,624,701 | |
| esv3809406 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 43,589,770 | 43,591,770 | 43,589,770 | 43,591,770 | - |
| esv3809406 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 31,775,635 | 31,777,635 | 31,775,635 | 31,777,635 | |||
| esv3809406 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 44,163,906 | 44,165,906 | 44,163,906 | 44,165,906 | - |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16638585 | interchromosomal translocation | 2120211 | Curated | Curated | 26 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv16638585 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 31,622,701 | 31,624,701 | 31,622,701 | 31,624,701 | not reported |
| essv16638585 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 43,589,770 | 43,591,770 | 43,589,770 | 43,591,770 | - |
| essv16638585 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 31,775,635 | 31,777,635 | 31,775,635 | 31,777,635 | not reported | ||
| essv16638585 | Submitted genomic | GRCh37 (hg19) | NC_000013.10 | Chr13 | 44,163,906 | 44,165,906 | 44,163,906 | 44,165,906 | - |