A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566151



Internal ID16006874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104992803..105089059hg38UCSC Ensembl
Innerchr14:105459140..105555396hg19UCSC Ensembl
Innerchr14:104530185..104626441hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3896257
hg1996257
hg1896257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834729
Samples
Known GenesC14orf79, CDCA4, GPR132
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566151
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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