A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066446



Internal ID18808977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19955845..20383956hg38UCSC Ensembl
Innerchr19:20066654..20494765hg19UCSC Ensembl
Innerchr19:19927654..20355765hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38428112
hg19428112
hg18428112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3456n100
Supporting Variantsnssv3723296
Samples
Known GenesZNF486, ZNF682, ZNF90
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066446
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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