A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059158



Internal ID18801689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19862680..20396193hg38UCSC Ensembl
Innerchr19:19973489..20576161hg19UCSC Ensembl
Innerchr19:19834489..20368001hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38533514
hg19602673
hg18533513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3456n100
Supporting Variantsnssv3569791
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF253, ZNF486, ZNF682, ZNF90, ZNF93
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059158
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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