A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562162



Internal ID16349571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68666813..68698681hg38UCSC Ensembl
Innerchr13:69240945..69272813hg19UCSC Ensembl
Innerchr13:68138946..68170814hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3831869
hg1931869
hg1831869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3226n54
Supporting Variantsnssv813452, nssv813453
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562162
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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