A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3365n100



Internal ID22789452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59539397..59562655hg38UCSC Ensembl
chr18:57206629..57229887hg19UCSC Ensembl
chr18:55357609..55380867hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3823259
hg1923259
hg1823259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061128, nsv1063351
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)dgv3365n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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