A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564879



Internal ID16352288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:58695198..58776766hg38UCSC Ensembl
Innerchr14:59161916..59243484hg19UCSC Ensembl
Innerchr14:58231669..58313237hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3881569
hg1981569
hg1881569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv828204
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564879
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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