A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566288



Internal ID16353697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105557737..105721893hg38UCSC Ensembl
Innerchr14:106024074..106188230hg19UCSC Ensembl
Innerchr14:105095119..105259275hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38164157
hg19164157
hg18164157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4001n54
Supporting Variantsnssv834966, nssv834965
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)nsv566288
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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