A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014098



Internal ID22075729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17034567..17037751hg38UCSC Ensembl
Outerchr4:17028780..17038211hg38UCSC Ensembl
Innerchr4:17036190..17039374hg19UCSC Ensembl
Outerchr4:17030403..17039834hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg389432
hg199432
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156118
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014098
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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