A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596619



Internal ID16037342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:356637..359059hg38UCSC Ensembl
Innerchr5:356752..359174hg19UCSC Ensembl
Innerchr5:409752..412174hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382423
hg192423
hg182423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9476n54
Supporting Variantsnssv1021063
Samples
Known GenesAHRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596619
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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