A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597159



Internal ID16384568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12616681..13032727hg38UCSC Ensembl
Innerchr5:12616793..13032839hg19UCSC Ensembl
Innerchr5:12669793..13085839hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38416047
hg19416047
hg18416047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1025301
Samples
Known GenesCT49
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597159
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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