A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566028



Internal ID16006751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103847686..103866422hg38UCSC Ensembl
Innerchr14:104314023..104332759hg19UCSC Ensembl
Innerchr14:103383776..103402512hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3818737
hg1918737
hg1818737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834413
Samples
Known GenesLINC00637
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566028
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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