A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv917n100



Internal ID22787004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67576984..67707282hg38UCSC Ensembl
chr10:69336742..69467040hg19UCSC Ensembl
chr10:69006748..69137046hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38130299
hg19130299
hg18130299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039680, nsv1035576, nsv1035301, nsv1051778, nsv1051902, nsv1046047, nsv1049368
Samples
Known GenesCTNNA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv917n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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