A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3651n100



Internal ID22789738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53435068..53520477hg38UCSC Ensembl
chr19:53938321..54023731hg19UCSC Ensembl
chr19:58630133..58715543hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3885410
hg1985411
hg1885411
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061401, nsv1067247, nsv1055350, nsv1058113, nsv1063557, nsv1062230, nsv1055382, nsv1066666, nsv1065230, nsv1066994
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3651n100
Frequency
Sample Size11257
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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