A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834342



Internal ID16128298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103520468..103522313hg38UCSC Ensembl
Innerchr14:103986805..103988650hg19UCSC Ensembl
Innerchr14:103056558..103058403hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381846
hg191846
hg181846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565991
Supporting Variants
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834342
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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