A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521686



Internal ID15448979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112656233..112670010hg38UCSC Ensembl
Innerchr13:113310547..113324324hg19UCSC Ensembl
Innerchr13:112358548..112372325hg18UCSC Ensembl
Innerchr13:112358548..112372325hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3813778
hg1913778
hg1813778
hg1713778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698306
Samples
Known GenesC13orf35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521686
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer