A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596617



Internal ID16037340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:356483..359196hg38UCSC Ensembl
Innerchr5:356598..359311hg19UCSC Ensembl
Innerchr5:409598..412311hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382714
hg192714
hg182714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9476n54
Supporting Variantsnssv1021058, nssv1021060, nssv1021061, nssv1021057, nssv1021059
Samples
Known GenesAHRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596617
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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