A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154623



Internal ID22085128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76153816..76216696hg38UCSC Ensembl
Outerchr10:76151274..76224619hg38UCSC Ensembl
Innerchr10:77913574..77976454hg19UCSC Ensembl
Outerchr10:77911032..77984377hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3873346
hg1973346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005886
Samples
Known GenesC10orf11
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154623
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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