esv3806706
- 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:Chr6:g.o(146222365_146224365)_chr10:(23161228_
23163228)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: 66 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 39 SVs from 14 studies. See in: genome view
Overlapping variant regions from other studies: 66 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 39 SVs from 14 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| esv3806706 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 145,901,229 | 145,903,229 | 145,901,229 | 145,903,229 | - |
| esv3806706 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 22,872,299 | 22,874,299 | 22,872,299 | 22,874,299 | |
| esv3806706 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 146,222,365 | 146,224,365 | 146,222,365 | 146,224,365 | - | ||
| esv3806706 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 23,161,228 | 23,163,228 | 23,161,228 | 23,163,228 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16635567 | interchromosomal translocation | 2120204 | Curated | Curated | 39 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv16635567 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 145,901,229 | 145,903,229 | 145,901,229 | 145,903,229 | - |
| essv16635567 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 22,872,299 | 22,874,299 | 22,872,299 | 22,874,299 | not reported |
| essv16635567 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 146,222,365 | 146,224,365 | 146,222,365 | 146,224,365 | - | ||
| essv16635567 | Submitted genomic | GRCh37 (hg19) | NC_000010.10 | Chr10 | 23,161,228 | 23,163,228 | 23,161,228 | 23,163,228 | not reported |