A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566278



Internal ID16353687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105543235..105671130hg38UCSC Ensembl
Innerchr14:106009572..106137467hg19UCSC Ensembl
Innerchr14:105080617..105208512hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38127896
hg19127896
hg18127896
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834952, nssv834953
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566278
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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