A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562159



Internal ID16349568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68666813..68693849hg38UCSC Ensembl
Innerchr13:69240945..69267981hg19UCSC Ensembl
Innerchr13:68138946..68165982hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3827037
hg1927037
hg1827037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3226n54
Supporting Variantsnssv813446, nssv813445, nssv813447
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562159
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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