A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566283



Internal ID16353692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105546146..105699778hg38UCSC Ensembl
Innerchr14:106012483..106166115hg19UCSC Ensembl
Innerchr14:105083528..105237160hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38153633
hg19153633
hg18153633
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4001n54
Supporting Variantsnssv834960
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)nsv566283
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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