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titleWelcome to HGVA project!

Human Genomic Variation Archive (HGVA) is an open access genomic variation resource that integrates all variants from key world-wide reference projects, but also added-value information such as basic variant annotation, population frequencies, protein effect predictions, variant-associated phenotype, etc.

HGVA is developed and maintained at University of Cambridge and it is available at http://bioinfodev.hpc.cam.ac.uk/web-apps/hgva

HGVA currently hosts about 400GB of data from more than 10 different studies describing more than 300 million unique variants. HGVA is not a mere data archive, but a big data provider that enables users to efficiently query, filter and retrieve relevant information from its knowledge-base, either from a visual web-based application or programmatically using RESTful web services.

Main Features

  • Most important high-quality variant studies normalised and integrated in just one server database
  • Rich variant annotation performed
  • Population frequencies calculated
  • Interactive web-based data mining tool based on IVA

Contact

  • Javier Lopez (javier.lopez@genomicsengland.co.uk)
  • Ignacio Medina (im411@cam.ac.uk)


Latest news:

Blog Posts
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Current Studies

Refernce Studies GRCh37

  • 1000 Genomes Phase 3
  • Exome Aggregation Consortium (ExAC)
  • Exome Sequencing Project (ESP6500)
  • Genome of the Netherlands(GoNL)
  • UK10K project
  • Spanish Medical Genome Project

Refernce Studies GRCh38

  • 1000 Genomes Phase 3

Cancer GRCh37

  • QIMR Berghofer Melanoma
  • Chronic Myeloid Leukemia - Russian Academy of Medical Sciences

Statistics

More than 500M variants reported and about 300M of unique variants


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titleVariant Studies GCh37


StudyNum. variants
1000G80000000
ExAC

63000000

ESP650010000000



Developers

Source Code

Web based on IVA project at  https://github.com/opencb/iva/tree/app/hgva

Server based on OpenCGA at  https://github.com/opencb/opencga

Contributing

HGVA is a collaborative project that aims to integrate as many reference human studies as possible, you can contact us for feature request. If you want to contribute to the code you are more than welcome to contribute to IVA and OpenCGA



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