A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520218



Internal ID15100825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:146654928..146668814hg38UCSC Ensembl
Innerchr5:146034491..146048377hg19UCSC Ensembl
Innerchr5:146014684..146028570hg18UCSC Ensembl
Innerchr5:146014684..146028570hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3813887
hg1913887
hg1813887
hg1713887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv356n21
Supporting Variantsnssv697398, nssv671592, nssv661965
Samples
Known GenesPPP2R2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520218
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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