A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566033



Internal ID16353442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104200484..104281047hg38UCSC Ensembl
Innerchr14:104666821..104747384hg19UCSC Ensembl
Innerchr14:103736574..103818429hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3880564
hg1980564
hg1881856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3948n54
Supporting Variantsnssv834418
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566033
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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