A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597433



Internal ID16384842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20940020..21069254hg38UCSC Ensembl
Innerchr5:20940129..21069363hg19UCSC Ensembl
Innerchr5:20975886..21105120hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38129235
hg19129235
hg18129235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9645n54
Supporting Variantsnssv1026840
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597433
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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