A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521771



Internal ID15102378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107719609..108033920hg38UCSC Ensembl
Innerchr11:107590335..107904646hg19UCSC Ensembl
Innerchr11:107095545..107409856hg18UCSC Ensembl
Innerchr11:107095545..107409856hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38314312
hg19314312
hg18314312
hg17314312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694538
Samples
Known GenesCUL5, RAB39A, SLC35F2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521771
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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