A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156154



Internal ID22086659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43377418..43423145hg38UCSC Ensembl
Outerchr4:43374475..43426409hg38UCSC Ensembl
Innerchr4:43379435..43425162hg19UCSC Ensembl
Outerchr4:43376492..43428426hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3851935
hg1951935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014246
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156154
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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