A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597153



Internal ID16384562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:11571828..12022586hg38UCSC Ensembl
Innerchr5:11571940..12022698hg19UCSC Ensembl
Innerchr5:11624940..12075698hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38450759
hg19450759
hg18450759
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1025296
Samples
Known GenesCTNND2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597153
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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