A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834953



Internal ID16128909
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
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566278
Supporting Variants
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)nssv834953
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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