A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562235



Internal ID16349644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70161932..70200674hg38UCSC Ensembl
Innerchr13:70736064..70774806hg19UCSC Ensembl
Innerchr13:69634065..69672807hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3838743
hg1938743
hg1838743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3237n54
Supporting Variantsnssv813763, nssv813764, nssv813762, nssv813761, nssv813760, nssv813765
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562235
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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