About this document
cbb752 26m6b 1000G PCAWG by sz477 is a document available to read on EtoBox.
The document summarizes human germline and somatic variation data, highlighting the significant increase in structural variants (SVs) from the 1000 Genomes Project (1000GP) to the Genome Aggregation Database (gnomAD). It discusses the prevalence of common and rare variants, the classification of variants in cancer genomes, and the goals of the Pan-Cancer Analysis of Whole Genomes (PCAWG) project. The document includes references to key studies and data sources related to human genetic variation.
- Author
- sz477
- Language
- EN