Concepedia

Copy Number Variant Databases

Copy Number Variant Databases is a curated genomic resource that systematically archives and provides access to experimentally derived or computationally predicted copy number variations across individuals and populations, distinguished by its focus on structural genomic alterations involving duplications or deletions of DNA segments.

40

Publications

4.4K

Citations

336

Authors

144

Institutions

Publications per year

2017–2026

13

Parents

Publications

40

The Database of Genomic Variants: a curated collection of structural variation in the human genome

Jeffrey R. MacDonald, Robert Ziman, Ryan K. C. Yuen et al. · Nucleic Acids Research · 2013 · 1.4K citations · Full text

, , +17

High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications

Tamim H. Shaikh, Xiaowu Gai, Juan C. Perín et al. · Genome Research · 2009 · 389 citations · Full text

, , +17

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

George Kirov, Dilihan Gumus, Wei Chen et al. · Human Molecular Genetics · 2007 · 381 citations · Full text

, , +16

dbVar and DGVa: public archives for genomic structural variation

Ilkka Lappalainen, John Lopez, Lisa Skipper et al. · Nucleic Acids Research · 2012 · 320 citations · Full text

, , +16

DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation

Eugene Bragin, Eleni Anthippi Chatzimichali, Caroline F. Wright et al. · Nucleic Acids Research · 2013 · 237 citations · Full text

, , +17

1–5 of 40

Authors

336

  1. HV
    Helen V. Firth

    Wellcome Sanger Institute, United Kingdom

    3 publications · 360 citations

    3

    h-index

  2. MS
    Mark Seielstad

    Genome Institute of Singapore, Singapore

    2 publications · 59 citations

    2

    h-index

  3. AP
    A. Paul Bevan

    University of Cambridge, United Kingdom

    2 publications · 252 citations

    2

    h-index

  4. LF
    Lars Feuk

    Uppsala University, Sweden

    2 publications · 1.5K citations

    2

    h-index

  5. RT
    Rick Twee‐Hee Ong

    National University of Singapore, Singapore

    2 publications · 59 citations

    2

    h-index

1–5 of 336

Institutions

144

  1. University of California, San Francisco

    San Francisco, United States

    4 h-index

    8 publications

    140 citations

  2. Addenbrooke's Hospital

    Cambridge, United Kingdom

    3 h-index

    9 publications

    1.8K citations

  3. Wellcome Sanger Institute

    Cambridge, United Kingdom

    3 h-index

    14 publications

    1.9K citations

  4. University of Pennsylvania

    Philadelphia, United States

    2 h-index

    11 publications

    3.6K citations

  5. Agency for Science, Technology and Research

    Singapore, Singapore

    2 h-index

    5 publications

    150 citations

  6. Harvard University

    Cambridge, United States

    2 h-index

    8 publications

    248 citations

  7. Cambridge University Hospitals NHS Foundation Trust

    Cambridge, United Kingdom

    2 h-index

    2 publications

    123 citations

  8. SickKids Foundation

    Toronto, Canada

    2 h-index

    6 publications

    7.1K citations

1–8 of 144

Venues

  1. Human Mutation

    5 publications · 322 citations

    5

    h-index

  2. Nucleic Acids Research

    4 publications · 2K citations

    4

    h-index

  3. PLoS ONE

    3 publications · 99 citations

    3

    h-index

  4. Scientific Reports

    2 publications · 149 citations

    2

    h-index

  5. BMC Genomics

    2 publications · 91 citations

    2

    h-index

1–5