A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1178n100



Internal ID20152794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55593873..55695666hg38UCSC Ensembl
chr11:55361349..55463142hg19UCSC Ensembl
chr11:55117925..55219718hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38101794
hg19101794
hg18101794
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053378, nsv1036981, nsv1046927, nsv1045061, nsv1042485, nsv1037738
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1178n100
Frequency
Sample Size29084
Observed Gain8
Observed Loss12
Observed Complex0
Frequencyn/a


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