A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596620



Internal ID16037343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:357491..359196hg38UCSC Ensembl
Innerchr5:357606..359311hg19UCSC Ensembl
Innerchr5:410606..412311hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381706
hg191706
hg181706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9477n54
Supporting Variantsnssv1021065, nssv1021064
Samples
Known GenesAHRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596620
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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