A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154962



Internal ID22085467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:93164040..93191168hg38UCSC Ensembl
Outerchr13:93161773..93196382hg38UCSC Ensembl
Innerchr13:93816293..93843421hg19UCSC Ensembl
Outerchr13:93814026..93848635hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3834610
hg1934610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008290
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154962
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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