A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579913



Internal ID16020636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50020969..50060642hg38UCSC Ensembl
Innerchr19:50524226..50563899hg19UCSC Ensembl
Innerchr19:55216038..55255711hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3839674
hg1939674
hg1839674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150655
Samples1780862432_A
Known GenesFLJ26850, VRK3, ZNF473
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579913
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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