A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3307n100



Internal ID20154923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:469797..683607hg38UCSC Ensembl
chr18:469797..683607hg19UCSC Ensembl
chr18:459797..673607hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38213811
hg19213811
hg18213811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067435, nsv1059242
Samples
Known GenesC18orf56, CETN1, CLUL1, COLEC12, ENOSF1, TYMS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3307n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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