A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579928



Internal ID16367337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50574798..50583776hg38UCSC Ensembl
Innerchr19:51078055..51087033hg19UCSC Ensembl
Innerchr19:55769867..55778845hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg388979
hg198979
hg188979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv900119
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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