A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014094



Internal ID22075725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10560127..10644396hg38UCSC Ensembl
Outerchr4:10558193..10647243hg38UCSC Ensembl
Innerchr4:10561751..10646020hg19UCSC Ensembl
Outerchr4:10559817..10648867hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3889051
hg1989051
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156114
Supporting Variants
Samples
Known GenesCLNK
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014094
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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