A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066564



Internal ID18809095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19945539..20415952hg38UCSC Ensembl
Innerchr19:20056348..20598758hg19UCSC Ensembl
Innerchr19:19917348..20390598hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38470414
hg19542411
hg18473251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3456n100
Supporting Variantsnssv3569792
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF682, ZNF826P, ZNF90
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066564
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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