A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593209



Internal ID16380618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:692774..754022hg38UCSC Ensembl
Innerchr4:686563..747810hg19UCSC Ensembl
Innerchr4:676563..737810hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3861249
hg1961248
hg1861248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv987413
Samples
Known GenesPCGF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593209
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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