A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705130



Internal ID15441782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:11529181..11539683hg38UCSC Ensembl
Innerchr5:11529293..11539795hg19UCSC Ensembl
Innerchr5:11582293..11592795hg18UCSC Ensembl
Innerchr5:11582293..11592795hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3810503
hg1910503
hg1810503
hg1710503
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528520
Supporting Variants
Samples
Known GenesCTNND2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705130
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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