A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585190



Internal ID16372599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:642066..648070hg38UCSC Ensembl
Innerchr20:622710..628714hg19UCSC Ensembl
Innerchr20:570710..576714hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386005
hg196005
hg186005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7424n54
Supporting Variantsnssv935338
Samples
Known GenesSRXN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585190
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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