A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5872n100



Internal ID20157488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:231934..397937hg38UCSC Ensembl
chr6:231934..397937hg19UCSC Ensembl
chr6:176934..342937hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38166004
hg19166004
hg18166004
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019602, nsv1025748, nsv1023605, nsv1019333, nsv1022334, nsv1030097, nsv1028184, nsv1019286, nsv1028848, nsv1031805, nsv1029392, nsv1015323, nsv1035064
Samples
Known GenesDUSP22, IRF4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5872n100
Frequency
Sample Size29084
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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