esv3788789
- 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:205,055
- Description:Chr16:g.26598737_26803791inv
- 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: 613 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 613 SVs from 63 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3788789 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 26,587,416 | 26,792,470 |
| esv3788789 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 26,598,737 | 26,803,791 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16615595 | inversion | 1737646 | Curated | Curated | 15 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16615595 | Remapped | Perfect | NC_000016.10:g.265 87416_26792470inv | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 26,587,416 | 26,792,470 |
| essv16615595 | Submitted genomic | NC_000016.9:g.2659 8737_26803791inv | GRCh37 (hg19) | NC_000016.9 | Chr16 | 26,598,737 | 26,803,791 |