A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566152



Internal ID16006875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104992803..105151554hg38UCSC Ensembl
Innerchr14:105459140..105617891hg19UCSC Ensembl
Innerchr14:104530185..104688936hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38158752
hg19158752
hg18158752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834730
Samples
Known GenesC14orf79, CDCA4, GPR132, JAG2, MIR6765
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566152
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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