A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566092



Internal ID16353501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104807749..104819994hg38UCSC Ensembl
Innerchr14:105274086..105286331hg19UCSC Ensembl
Innerchr14:104345131..104357376hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3812246
hg1912246
hg1812246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834625
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566092
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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