A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562269



Internal ID16349678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71527229..71622849hg38UCSC Ensembl
Innerchr13:72101361..72196981hg19UCSC Ensembl
Innerchr13:70999362..71094982hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3895621
hg1995621
hg1895621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3242n54
Supporting Variantsnssv813826
Samples
Known GenesDACH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562269
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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