esv3799653
- 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:Chr8:g.o(102223558_102223958)_chr8:o(102651536
_102651936)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: 94 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 90 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 94 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 90 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| esv3799653 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 101,211,330 | 101,211,730 | 101,211,330 | 101,211,730 | - |
| esv3799653 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 101,639,308 | 101,639,708 | 101,639,308 | 101,639,708 | - |
| esv3799653 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 102,223,558 | 102,223,958 | 102,223,558 | 102,223,958 | - | ||
| esv3799653 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 102,651,536 | 102,651,936 | 102,651,536 | 102,651,936 | - |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16627701 | intrachromosomal translocation | 1126524 | Curated | Curated | 93 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv16627701 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 101,211,330 | 101,211,730 | 101,211,330 | 101,211,730 | - |
| essv16627701 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 101,639,308 | 101,639,708 | 101,639,308 | 101,639,708 | - |
| essv16627701 | Submitted genomic | GRCh37 (hg19) | NC_000008.10 | Chr8 | 102,223,558 | 102,223,958 | 102,223,558 | 102,223,958 | - | ||
| essv16627701 | Submitted genomic | GRCh37 (hg19) | NC_000008.10 | Chr8 | 102,651,536 | 102,651,936 | 102,651,536 | 102,651,936 | - |