esv3768889
- 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:423,313
- Description:Chr13:g.83582511_84005823inv
- Publication(s):Bass 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: 1386 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 1386 SVs from 83 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3768889 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 83,008,376 | 83,431,688 |
| esv3768889 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 83,582,511 | 84,005,823 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16593453 | inversion | 1565440 | Curated | Curated | 180 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16593453 | Remapped | Perfect | NC_000013.11:g.830 08376_83431688inv | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 83,008,376 | 83,431,688 |
| essv16593453 | Submitted genomic | NC_000013.10:g.835 82511_84005823inv | GRCh37 (hg19) | NC_000013.10 | Chr13 | 83,582,511 | 84,005,823 |