A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3514n100



Internal ID22789601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33712542..33743652hg38UCSC Ensembl
chr19:34203447..34234557hg19UCSC Ensembl
chr19:38895287..38926397hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3831111
hg1931111
hg1831111
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062383, nsv1064064, nsv1066675
Samples
Known GenesCHST8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3514n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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