esv3790426
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:inversion
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:108,925
- Description:Chr8:g.143007429_143116353inv
- Publication(s):Bass et al. 2011, 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: 573 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 573 SVs from 70 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3790426 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 141,926,068 | 142,034,992 |
| esv3790426 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 143,007,429 | 143,116,353 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16617399 | inversion | 1565439 | Curated | Curated | 68 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16617399 | Remapped | Perfect | NC_000008.11:g.141 926068_142034992in v | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 141,926,068 | 142,034,992 |
| essv16617399 | Submitted genomic | NC_000008.10:g.143 007429_143116353in v | GRCh37 (hg19) | NC_000008.10 | Chr8 | 143,007,429 | 143,116,353 |