A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518082



Internal ID15098689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98665259..98684036hg38UCSC Ensembl
Innerchr13:99317513..99336290hg19UCSC Ensembl
Innerchr13:98115514..98134291hg18UCSC Ensembl
Innerchr13:98115514..98134291hg17UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3818778
hg1918778
hg1818778
hg1718778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695495
Samples
Known GenesSLC15A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518082
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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