A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156116



Internal ID22086621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10734386..10766387hg38UCSC Ensembl
Outerchr4:10731576..10769476hg38UCSC Ensembl
Innerchr4:10736010..10768011hg19UCSC Ensembl
Outerchr4:10733200..10771100hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3837901
hg1937901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014096
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156116
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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