dbVar: Study Browser
| Date | Publication | Study | Organism | Variant Region Count | Variant Call Count |
|---|---|---|---|---|---|
| 2023/10 | Clinical Structural Variants | nstd102 | Human | 83,844 | 88,454 |
| 2019/05 | Frenkel et al. 2019 | nstd157 | Human | 1,907 | 4,402 |
| 2017/02 | Walker et al. 2017 | nstd132 | Human | 6,173 | 15,888 |
| 2016/08 | Exome Aggregation Consortium CNVs | nstd151 | Human | 49,339 | 126,771 |
| 2015/08 | Polyak et al. 2015 | nstd113 | Human | 9,010 | 16,828 |
| 2015/01 | Simpson et al. 2015 | estd218 | Human | 5,513 | 5,513 |
| 2013/08 | de Ligt et al. 2013 | nstd84 | Human | 10,376 | 11,064 |
| 2013/05 | Boone et al. 2013 | nstd80 | Human | 1,512 | 3,785 |
| 2008/01 | Marshall et al. 2008 | nstd12 | Human | 2,290 | 3,396 |
- SNP array (3)
- Oligo aCGH (2)
- Multiple (1)
- Oligo aCGH, SNP array, Sequencing (1)
- SNP array, qPCR (1)
- Sequencing (1)
Source: NCBI