A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156264



Internal ID22084740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:169050728..169074827hg38UCSC Ensembl
Outerchr4:169047435..169076747hg38UCSC Ensembl
Innerchr4:169971879..169995978hg19UCSC Ensembl
Outerchr4:169968586..169997898hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3829313
hg1929313
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016965
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156264
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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