esv3781922
- 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:94,894
- Description:Chr16:g.3879875_3784982inv
- Publication(s):Forbes et al. 2008, Forbes et al. 2008, Robinson 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: 349 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 349 SVs from 41 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3781922 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 3,734,981 | 3,829,874 |
| esv3781922 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 3,784,982 | 3,879,875 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16607980 | inversion | 1732892 | Curated | Curated | 8 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16607980 | Remapped | Perfect | NC_000016.10:g.373 4981_3829874inv | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 3,734,981 | 3,829,874 |
| essv16607980 | Submitted genomic | NC_000016.9:g.3784 982_3879875inv | GRCh37 (hg19) | NC_000016.9 | Chr16 | 3,784,982 | 3,879,875 |