A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596616



Internal ID16037339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:356266..410932hg38UCSC Ensembl
Innerchr5:356381..411047hg19UCSC Ensembl
Innerchr5:409381..464047hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3854667
hg1954667
hg1854667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1021056
Samples
Known GenesAHRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596616
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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