A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566297



Internal ID16353706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105574055..105723956hg38UCSC Ensembl
Innerchr14:106040392..106190293hg19UCSC Ensembl
Innerchr14:105111437..105261338hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38149902
hg19149902
hg18149902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4001n54
Supporting Variantsnssv834976
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)nsv566297
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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