1000 Genomes Project (human) 321 0

2019-08-02

Creator: zhanglei2@genomics.cn

The purpose of the 1000 Genomes Project (human) is to support the discovery and understanding of genetic variants that influence human disease. Specifically defined goals are (a) the discovery of single nucleotide variants at frequencies of 1% or higher in diverse populations, (b) even more comprehensive discovery (variants down to frequencies of 0.1 - 0.5%) in functional gene regions, and (c) discovery of structural variants, such as copy number variants, other insertions and deletions, and inversions, including sequence-level understanding of breakpoints.

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  Source:  CNGB Project  ( ID CNPhis0002809 )

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https://db.cngb.org
https://db.cngb.org/data_access/

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  Source:  CNGB Project  ( ID CNPhis0002858 )

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https://db.cngb.org
https://db.cngb.org/data_access/

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  Source:  CNGB Project  ( ID CNPhis0003309 )

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https://db.cngb.org
https://db.cngb.org/data_access/

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Other details

Referenced accession ID :

The dataset references CNPhis0002809, CNPhis0002858, CNPhis0003309, CNPhis0003097, CNPhis0003095, CNPhis0003083, CNPhis0003094, CNPhis0000001, CNPhis0002830, CNPhis0000002, thanks to the submitters and researchers of the data.

How to site the dataset :

To respect the results of the dataset creator and updater, it is recommended to reference the dataset accession ID in the article :

The dataset that support this study is DATAXXXXXX which was created in CNGBdb(https://db.cngb.org)

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