A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562276



Internal ID16349685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71571206..71666431hg38UCSC Ensembl
Innerchr13:72145338..72240563hg19UCSC Ensembl
Innerchr13:71043339..71138564hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3895226
hg1995226
hg1895226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3243n54
Supporting Variantsnssv1175998
SamplesNINDS_189
Known GenesDACH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562276
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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