A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579998



Internal ID16020721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51767689..52109852hg38UCSC Ensembl
Innerchr19:52270942..52613105hg19UCSC Ensembl
Innerchr19:56962754..57304917hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38342164
hg19342164
hg18342164
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6523n54
Supporting Variantsnssv900958
Samples
Known GenesFPR2, FPR3, HCCAT3, ZNF350, ZNF432, ZNF577, ZNF613, ZNF614, ZNF615, ZNF649, ZNF841
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579998
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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