A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3465n100



Internal ID20155081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20420512..20626420hg38UCSC Ensembl
chr19:20603318..20809226hg19UCSC Ensembl
chr19:20395158..20601066hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38205909
hg19205909
hg18205909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060008, nsv1063433
Samples
Known GenesZNF626, ZNF737, ZNF826P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3465n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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