A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523242



Internal ID15450535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103032716..103050314hg38UCSC Ensembl
Innerchr13:103685066..103702664hg19UCSC Ensembl
Innerchr13:102483067..102500665hg18UCSC Ensembl
Innerchr13:102483067..102500665hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3817599
hg1917599
hg1817599
hg1717599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698970
Samples
Known GenesSLC10A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523242
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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