HGVA specifications

Unique identifier:
OMICS_18704
Restrictions to use:
None
Community driven:
No
User data submission:
Not allowed
Maintained:
Yes
Name:
Human Genome Variation Archive
Database management system:
NoSQL
Data access:
File download, Browse
Version:
1.1.0

HGVA support

Maintainers

  • Ignacio Medina <>
  • Javier Lopez <>
  • Joaquin Dopazo <>

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Publications

Institution(s)

Genomics England, Charterhouse Square, London, UK; Department of Haematology, University of Cambridge, Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK; NIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge Biomedical Campus, Cambridge, UK; HPC Service, UIS, University of Cambridge, Cambridge, UK; Clinical Bioinformatics Area, Fundacion Progreso y Salud (FPS), Hospital Virgen del Rocio, Sevilla, Spain; Functional Genomics Node (INB), FPS, Hospital Virgen del Rocio, Sevilla, Spain; Bioinformatics in Rare Diseases (BiER), Centro de Investigacion Biomedica en Red de Enfermedades Raras (CIBERER), FPS, Hospital Virgen del Rocio, Sevilla, Spain

Funding source(s)

Supported by Spanish Ministry of Economy and Competitiveness [BIO2014-57291-R, in part]; Instituto de Salud Carlos III (ISCIII) Plataforma de Recursos Biomoleculares y Bioinformaticos [PT13/0001/0007]; European Regional Development Funds (ERDF) [EU H2020-INFRADEV-1- 2015-1 ELIXIR-EXCELERATE (ref. 676559)]; National Institute for Health Research (NIHR) England [RG65966].

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