A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520071



Internal ID15100678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:146655993..146671213hg38UCSC Ensembl
Innerchr5:146035556..146050776hg19UCSC Ensembl
Innerchr5:146015749..146030969hg18UCSC Ensembl
Innerchr5:146015749..146030969hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3815221
hg1915221
hg1815221
hg1715221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv356n21
Supporting Variantsnssv697208
Samples
Known GenesPPP2R2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520071
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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