A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596589



Internal ID16383998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12225..66289hg38UCSC Ensembl
Innerchr5:12225..66404hg19UCSC Ensembl
Innerchr5:65225..119404hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3854065
hg1954180
hg1854180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1021026
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596589
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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