A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596591



Internal ID16384000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:27565..118291hg38UCSC Ensembl
Innerchr5:27564..118406hg19UCSC Ensembl
Innerchr5:80564..171406hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3890727
hg1990843
hg1890843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153274
SamplesHGDP00099
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596591
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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