esv3793215
- 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:
Chr9:g.o(22928416_22928816)_chr9:(22934049_22934449)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: 255 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 236 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 259 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 240 SVs from 35 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| esv3793215 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 22,928,417 | 22,928,817 | 22,928,417 | 22,928,817 | - |
| esv3793215 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 22,934,050 | 22,934,450 | 22,934,050 | 22,934,450 | |
| esv3793215 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 22,928,416 | 22,928,816 | 22,928,416 | 22,928,816 | - | ||
| esv3793215 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 22,934,049 | 22,934,449 | 22,934,049 | 22,934,449 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16620507 | intrachromosomal translocation | 749715 | Curated | Curated | 91 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv16620507 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 22,928,417 | 22,928,817 | 22,928,417 | 22,928,817 | - |
| essv16620507 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 22,934,050 | 22,934,450 | 22,934,050 | 22,934,450 | not reported |
| essv16620507 | Submitted genomic | GRCh37 (hg19) | NC_000009.11 | Chr9 | 22,928,416 | 22,928,816 | 22,928,416 | 22,928,816 | - | ||
| essv16620507 | Submitted genomic | GRCh37 (hg19) | NC_000009.11 | Chr9 | 22,934,049 | 22,934,449 | 22,934,049 | 22,934,449 | not reported |