A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv356n21



Internal ID20132077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146654928..146671213hg38UCSC Ensembl
chr5:146034491..146050776hg19UCSC Ensembl
chr5:146014684..146030969hg18UCSC Ensembl
chr5:146014684..146030969hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3816286
hg1916286
hg1816286
hg1716286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520218, nsv520071
Samples
Known GenesPPP2R2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv356n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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