A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8164n54



Internal ID20141588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1907610..2478272hg38UCSC Ensembl
chr3:1949294..2519956hg19UCSC Ensembl
chr3:1924294..2494956hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38570663
hg19570663
hg18570663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589367, nsv589366
Samples1780862435_A
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8164n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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