A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016962



Internal ID22078593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167288746..167347085hg38UCSC Ensembl
Outerchr4:167275922..167359206hg38UCSC Ensembl
Innerchr4:168209897..168268236hg19UCSC Ensembl
Outerchr4:168197073..168280357hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3883285
hg1983285
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156261
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4016962
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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