A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579050



Internal ID16366459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23525864..23888352hg38UCSC Ensembl
Innerchr19:23708666..24071154hg19UCSC Ensembl
Innerchr19:23500506..23862994hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38362489
hg19362489
hg18362489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6344n54
Supporting Variantsnssv896913
Samples
Known GenesRPSAP58, ZNF675, ZNF681
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579050
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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