A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3495n100



Internal ID22789582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27257073..27466119hg38UCSC Ensembl
chr19:27747981..27957027hg19UCSC Ensembl
chr19:32439821..32648867hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38209047
hg19209047
hg18209047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059622, nsv1064163
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)dgv3495n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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