A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596890



Internal ID16037613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1820443..1855187hg38UCSC Ensembl
Innerchr5:1820557..1855301hg19UCSC Ensembl
Innerchr5:1873557..1908301hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3834745
hg1934745
hg1834745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153526
SamplesNINDS_50
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596890
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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