A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3499n100



Internal ID22789586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27257073..27704107hg38UCSC Ensembl
chr19:27747981..28195015hg19UCSC Ensembl
chr19:32439821..32886855hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38447035
hg19447035
hg18447035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062493, nsv1056628, nsv1067376, nsv1060972, nsv1064177, nsv1066251, nsv1060114
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)dgv3499n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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