A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3366n100



Internal ID22789453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59679539..59744183hg38UCSC Ensembl
chr18:57346771..57411415hg19UCSC Ensembl
chr18:55497751..55562395hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3864645
hg1964645
hg1864645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059252, nsv1057526
Samples
Known GenesCCBE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3366n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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