A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3011n100



Internal ID20154627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70102965..70212424hg38UCSC Ensembl
chr16:70136868..70246327hg19UCSC Ensembl
chr16:68694369..68803828hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38109460
hg19109460
hg18109460
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058087, nsv1057267
Samples
Known GenesCLEC18C, PDPR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3011n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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