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 variations (CNVs) identified in Korean individuals.

BMC genomics - 18 Oct 2008

Kang Tae-Wook, Jeon Yeo-Jin, Jang Eunsu, Kim Hee-Jin, Kim Jeong-Hwan, Park Jong-Lyul, Lee Siwoo, Kim Yong Sung, Kim Jong Yeol, Kim Seon-Young

Abstract excerpt

BACKGROUND: Copy number variations (CNVs) are deletions, insertions, duplications, and more complex variations ranging from 1 kb to sub-microscopic sizes. Recent advances in array technologies have enabled researchers to identify a number of CNVs from normal individuals. However, the identification of new CNVs has not yet reached saturation, and more CNVs from diverse populations remain to be discovered. RESULTS:...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Gene Dosage
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetics, Population

Share to Genome, Human

Share to Oligonucleotide Array Sequence Analysis

Source

Open in PubMed Open full text

Identifiers

PMID: 18928558
DOI: 10.1186/1471-2164-9-492
PMCID: PMC2576253

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Copy number variations (CNVs) identified in Korean individuals.PMID 18928558Read ↗

KGVDB: a population-based genomic map of CNVs tagged by SNPs in Koreans.Semantic proximity Read ↗

A comprehensive profile of DNA copy number variations in a Korean population: identification of copy number invariant regions among Koreans.Semantic proximity Read ↗

Data-driven approach to detect common copy-number variations and frequency profiles in a population-based Korean cohort.Semantic proximity Read ↗

SgD-CNV, a database for common and rare copy number variants in three Asian populations.Semantic proximity Read ↗

A genome-wide survey of copy number variations in Han Chinese residing in Taiwan.Semantic proximity Read ↗

CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing.Semantic proximity Read ↗

Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing.Semantic proximity Read ↗

[Association of common copy number variations with diseases].Semantic proximity Read ↗

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

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations.Semantic proximity Read ↗

Whole genome distribution and ethnic differentiation of copy number variation in Caucasian and Asian populations.Semantic proximity Read ↗

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

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