A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566054



Internal ID16353463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104680242..104734040hg38UCSC Ensembl
Innerchr14:105146579..105200377hg19UCSC Ensembl
Innerchr14:104217624..104271422hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3853799
hg1953799
hg1853799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3954n54
Supporting Variantsnssv834435
Samples
Known GenesADSSL1, INF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566054
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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