A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5034n100



Internal ID22791121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195746913..195915321hg38UCSC Ensembl
chr3:195473784..195642192hg19UCSC Ensembl
chr3:196959455..197126589hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38168409
hg19168409
hg18167135
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003062, nsv997893
Samples
Known GenesMIR6829, MUC4, TNK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5034n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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