A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600325



Internal ID16387734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:174343553..174401952hg38UCSC Ensembl
Innerchr5:173770556..173828955hg19UCSC Ensembl
Innerchr5:173703162..173761561hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3858400
hg1958400
hg1858400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1045664
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600325
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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