A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563227



Internal ID16350636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112656233..112671625hg38UCSC Ensembl
Innerchr13:113310547..113325939hg19UCSC Ensembl
Innerchr13:112358548..112373940hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3815393
hg1915393
hg1815393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820154
Samples
Known GenesC13orf35
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563227
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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