A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562234



Internal ID16349643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70161932..70200338hg38UCSC Ensembl
Innerchr13:70736064..70774470hg19UCSC Ensembl
Innerchr13:69634065..69672471hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3838407
hg1938407
hg1838407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3237n54
Supporting Variantsnssv813759, nssv813757, nssv813758
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562234
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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