Database of genomic structural VARiation

dbVar is a database of human genomic structural variation where users can search, view, and download data from submitted studies. dbVar stopped supporting data from non-human organisms in 2017, however existing non-human data remains available. In keeping with the common definition of structural variation, most variants are larger than 50 basepairs in length - however a handful of smaller variants may also be found. dbVar provides access to the raw data whenever available, as well as links to additional resources, from both NCBI and elsewhere. It can accept diverse types of events, including inversions, insertions and translocations. Additionally, both germline and somatic variants are accepted.

dbVar是人类基因组结构变异数据库，用户可在此对已提交的研究数据进行检索、查看与下载。该数据库于2017年停止支持非人类生物的数据提交，但现有非人类数据仍可正常访问。按照结构变异的通用定义，绝大多数变异的长度均大于50个碱基对，但也可找到少量长度更小的变异。dbVar会在数据可用时提供原始数据访问权限，同时附带来自NCBI及其他渠道的额外资源链接。该数据库可收录多种类型的变异事件，包括倒位、插入与易位；此外，生殖系变异与体细胞变异均可被收录。

搜集汇总

背景与挑战

背景概述

dbVar是一个人类基因组结构变异数据库，收录了大于50个碱基对的结构变异数据，包括倒位、插入和易位等类型，并提供原始数据与相关资源链接。该数据库自2017年起仅支持人类数据，但仍可访问历史非人类数据。