A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150142



Internal ID15530761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52157026..52190024hg38UCSC Ensembl
Innerchr19:52660279..52693277hg19UCSC Ensembl
Innerchr19:57352091..57385089hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3832999
hg1932999
hg1832999
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580007
Supporting Variants
SamplesHGDP00993
Known GenesPPP2R1A, ZNF836
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150142
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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