Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Copy number variation and human genome maps.

Nature genetics - 1 May 2010

McCarroll Steven A

Abstract excerpt

Maps of human genome copy number variation (CNV) are maturing into useful resources for complex disease genetics. Four new studies increase the resolution of CNV maps and seek to locate human phenotypic variation on these maps.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genome, Human
Share to Genomics
Share to Linkage Disequilibrium
Share to Gene Dosage

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome

Share to Chromosome Mapping

Share to Epigenesis, Genetic

Share to Nucleic Acid Hybridization

Source

Identifiers

PMID: 20428091
DOI: 10.1038/ng0510-365

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Copy number variation and human genome maps.PMID 20428091Read ↗

A copy number variation map of the human genome.Semantic proximity Read ↗

Global variation in copy number in the human genome.Semantic proximity Read ↗

Copy number variations in the human genome and strategies for analysis.Semantic proximity Read ↗

Human copy number variation and complex genetic disease.Semantic proximity Read ↗

Copy number variation in human health, disease, and evolution.Semantic proximity Read ↗

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.Semantic proximity Read ↗

The impact of human copy number variation on a new era of genetic testingSemantic proximity Read ↗

Influences of rare copy number variation on human complex traitsSemantic proximity Read ↗

[Copy number variations in the human genome: their mutational mechanisms and roles in diseases].Semantic proximity Read ↗

Copy number variants, diseases and gene expression.Semantic proximity Read ↗

CNVs and genetic medicine (excitement and consequences of a rediscovery).Semantic proximity Read ↗

[Copy-number variation: a new pattern of structural diversity in genome].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.