A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834411



Internal ID16128367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103847246..103847686hg38UCSC Ensembl
Innerchr14:104313583..104314023hg19UCSC Ensembl
Innerchr14:103383336..103383776hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38441
hg19441
hg18441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566026
Supporting Variants
Samples
Known GenesPPP1R13B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834411
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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