A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151459



Internal ID15507080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:18890274..19046019hg38UCSC Ensembl
Innerchr22:18877787..19033532hg19UCSC Ensembl
Innerchr22:17257787..17413532hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38155746
hg19155746
hg18155746
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588180
Supporting Variants
Samples1780854430_A
Known GenesDGCR10, DGCR2, DGCR5, DGCR6, DGCR9, PRODH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151459
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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