A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066796



Internal ID18809327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50023786..50082619hg38UCSC Ensembl
Innerchr19:50527043..50585876hg19UCSC Ensembl
Innerchr19:55218855..55277688hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3858834
hg1958834
hg1858834
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3622n100
Supporting Variantsnssv3574988, nssv3574987
Samples
Known GenesFLJ26850, VRK3, ZNF473
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066796
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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