A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528827



Internal ID15109434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:146668814..146671213hg38UCSC Ensembl
Innerchr5:146048377..146050776hg19UCSC Ensembl
Innerchr5:146028570..146030969hg18UCSC Ensembl
Innerchr5:146028570..146030969hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382400
hg192400
hg182400
hg172400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705501
Samples
Known GenesPPP2R2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528827
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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