esv3798620
- 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:391,817
- Description:Chr6:g.62599113_62990929inv
- Publication(s):Forbes et al. 2008, Forbes et al. 2008, Fujimoto et al. 2012
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: 958 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 958 SVs from 72 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3798620 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 61,889,208 | 62,281,024 |
| esv3798620 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 62,599,113 | 62,990,929 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16626556 | inversion | 1737641 | Curated | Curated | 59 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16626556 | Remapped | Perfect | NC_000006.12:g.618 89208_62281024inv | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 61,889,208 | 62,281,024 |
| essv16626556 | Submitted genomic | NC_000006.11:g.625 99113_62990929inv | GRCh37 (hg19) | NC_000006.11 | Chr6 | 62,599,113 | 62,990,929 |