A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3336n100



Internal ID20154952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37368942..37407677hg38UCSC Ensembl
chr18:34948905..34987640hg19UCSC Ensembl
chr18:33202903..33241638hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3838736
hg1938736
hg1838736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055209, nsv1059042
Samples
Known GenesCELF4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3336n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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