A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024658



Internal ID19113875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:11743447..11850854hg38UCSC Ensembl
Innerchr5:11743559..11850966hg19UCSC Ensembl
Innerchr5:11796559..11903966hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38107408
hg19107408
hg18107408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3748678
Samples
Known GenesCTNND2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024658
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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