A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523326



Internal ID15450619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20618318..20623214hg38UCSC Ensembl
Innerchr11:20639864..20644760hg19UCSC Ensembl
Innerchr11:20596440..20601336hg18UCSC Ensembl
Innerchr11:20596440..20601336hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384897
hg194897
hg184897
hg174897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699070
Samples
Known GenesSLC6A5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523326
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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