A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562227



Internal ID16349636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70159712..70194552hg38UCSC Ensembl
Innerchr13:70733844..70768684hg19UCSC Ensembl
Innerchr13:69631845..69666685hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3834841
hg1934841
hg1834841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3237n54
Supporting Variantsnssv813742, nssv813741
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562227
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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