A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156141



Internal ID22086646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35401353..35533946hg38UCSC Ensembl
Outerchr4:35394098..35534187hg38UCSC Ensembl
Innerchr4:35402975..35535568hg19UCSC Ensembl
Outerchr4:35395720..35535809hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38140090
hg19140090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014232
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156141
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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