A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3401n100



Internal ID22789488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74355436..74453287hg38UCSC Ensembl
chr18:72022671..72120522hg19UCSC Ensembl
chr18:70173651..70271502hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3897852
hg1997852
hg1897852
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060332, nsv1057280
Samples
Known GenesC18orf63, FAM69C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3401n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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