A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596590



Internal ID16037313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12225..129591hg38UCSC Ensembl
Innerchr5:12225..129706hg19UCSC Ensembl
Innerchr5:65225..182706hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38117367
hg19117482
hg18117482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9471n54
Supporting Variantsnssv1021027
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596590
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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