A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066784



Internal ID18809315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12451697..12597468hg38UCSC Ensembl
Innerchr19:12562511..12708282hg19UCSC Ensembl
Innerchr19:12423511..12569282hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38145772
hg19145772
hg18145772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3436n100
Supporting Variantsnssv3564764
Samples
Known GenesZNF490, ZNF564, ZNF709
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066784
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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