A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2617n100



Internal ID22788704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70146176..70178938hg38UCSC Ensembl
chr15:70438515..70471277hg19UCSC Ensembl
chr15:68225569..68258331hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3832763
hg1932763
hg1832763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047020, nsv1041308
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2617n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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