A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3390n100



Internal ID20155006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68019389..68866022hg38UCSC Ensembl
chr18:65686626..66533259hg19UCSC Ensembl
chr18:63837606..64684239hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38846634
hg19846634
hg18846634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057034, nsv1056926
Samples
Known GenesCCDC102B, TMX3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3390n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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