A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2324n100



Internal ID19012692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20765925..20952464hg38UCSC Ensembl
chr15:20971254..21157793hg19UCSC Ensembl
chr15:19231299..19422452hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38186540
hg19186540
hg18191154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047772, nsv1042766, nsv1050007, nsv1038160
Samples
Known GenesCT60, CXADRP2, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2324n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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