esv3813603
- 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:401
- Description:Chr11:g.o(66569254_66569654)_chr11:o(67746006_
67746406)bkpt - Publication(s):Forbes et al. 2008, Forbes et al. 2008, Stephens et al. 2009
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: 57 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 148 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 57 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 148 SVs from 51 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| esv3813603 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 66,801,783 | 66,802,183 | 66,801,783 | 66,802,183 | - |
| esv3813603 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 67,978,535 | 67,978,935 | 67,978,535 | 67,978,935 | - |
| esv3813603 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 66,569,254 | 66,569,654 | 66,569,254 | 66,569,654 | - | ||
| esv3813603 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 67,746,006 | 67,746,406 | 67,746,006 | 67,746,406 | - |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16643353 | intrachromosomal translocation | 1126080 | Curated | Curated | 9 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv16643353 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 66,801,783 | 66,802,183 | 66,801,783 | 66,802,183 | - |
| essv16643353 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,978,535 | 67,978,935 | 67,978,535 | 67,978,935 | - |
| essv16643353 | Submitted genomic | GRCh37 (hg19) | NC_000011.9 | Chr11 | 66,569,254 | 66,569,654 | 66,569,254 | 66,569,654 | - | ||
| essv16643353 | Submitted genomic | GRCh37 (hg19) | NC_000011.9 | Chr11 | 67,746,006 | 67,746,406 | 67,746,006 | 67,746,406 | - |