A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5524n100



Internal ID22791611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:659283..825526hg38UCSC Ensembl
chr5:659398..825641hg19UCSC Ensembl
chr5:712398..878641hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38166244
hg19166244
hg18166244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029584, nsv1023445, nsv1020729, nsv1027846, nsv1018743, nsv1021350, nsv1015226, nsv1015821, nsv1019762, nsv1023689, nsv1021509, nsv1015814, nsv1025313, nsv1033635
Samples
Known GenesTPPP, ZDHHC11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5524n100
Frequency
Sample Size11257
Observed Gain40
Observed Loss0
Observed Complex0
Frequencyn/a


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