A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3400n100



Internal ID20155016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73757795..74189316hg38UCSC Ensembl
chr18:71425030..71856551hg19UCSC Ensembl
chr18:69576010..70007531hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38431522
hg19431522
hg18431522
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058258, nsv1060111, nsv1063130
Samples
Known GenesFBXO15, TIMM21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3400n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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