esv3778344
- 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:199,611
- Description:Chr7:g.80914275_81113885inv
- Publication(s):Berger 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: 473 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 473 SVs from 67 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3778344 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 81,284,959 | 81,484,569 |
| esv3778344 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 80,914,275 | 81,113,885 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16603997 | inversion | 1669606 | Curated | Curated | 116 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16603997 | Remapped | Perfect | NC_000007.14:g.812 84959_81484569inv | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 81,284,959 | 81,484,569 |
| essv16603997 | Submitted genomic | NC_000007.13:g.809 14275_81113885inv | GRCh37 (hg19) | NC_000007.13 | Chr7 | 80,914,275 | 81,113,885 |