A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579999



Internal ID16020722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51784199..52098146hg38UCSC Ensembl
Innerchr19:52287452..52601399hg19UCSC Ensembl
Innerchr19:56979264..57293211hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38313948
hg19313948
hg18313948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6523n54
Supporting Variantsnssv900959
Samples
Known GenesFPR3, 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)nsv579999
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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