A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154652



Internal ID22085157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:111147912..111183080hg38UCSC Ensembl
Outerchr10:111146320..111185723hg38UCSC Ensembl
Innerchr10:112907670..112942838hg19UCSC Ensembl
Outerchr10:112906078..112945481hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3839404
hg1939404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004465
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154652
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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