A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4634n100



Internal ID20156250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1974634..2157221hg38UCSC Ensembl
chr3:2016318..2198905hg19UCSC Ensembl
chr3:1991318..2173905hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38182588
hg19182588
hg18182588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006228, nsv1004360, nsv1007316
Samples
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4634n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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