A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526452



Internal ID15107059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110503272..110659020hg38UCSC Ensembl
Innerchr10:112263030..112418778hg19UCSC Ensembl
Innerchr10:112253020..112408768hg18UCSC Ensembl
Innerchr10:112253020..112408768hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38155749
hg19155749
hg18155749
hg17155749
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702755
Samples
Known GenesDUSP5, RBM20, SMC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526452
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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