A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3368n100



Internal ID22789455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59982075..59997780hg38UCSC Ensembl
chr18:57649307..57665012hg19UCSC Ensembl
chr18:55800287..55815992hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3815706
hg1915706
hg1815706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055317, nsv1063438, nsv1058868, nsv1063671, nsv1061766, nsv1065882, nsv1065219, nsv1064283, nsv1063675, nsv1066946, nsv1055250, nsv1057972, nsv1066114, nsv1067363
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3368n100
Frequency
Sample Size11257
Observed Gain53
Observed Loss0
Observed Complex0
Frequencyn/a


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