esv3809982
- 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:163,840
- Description:Chr7:g.4195367_4359205inv
- Publication(s):Berger et al. 2012, 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: 878 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 878 SVs from 74 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3809982 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 4,155,735 | 4,319,574 |
| esv3809982 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 4,195,367 | 4,359,205 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16639250 | inversion | 1673896 | Curated | Curated | 182 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16639250 | Remapped | Good | NC_000007.14:g.415 5735_4319574inv | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 4,155,735 | 4,319,574 |
| essv16639250 | Submitted genomic | NC_000007.13:g.419 5367_4359205inv | GRCh37 (hg19) | NC_000007.13 | Chr7 | 4,195,367 | 4,359,205 |