A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522240



Internal ID15449533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42930731..42951703hg38UCSC Ensembl
Innerchr11:42952281..42973253hg19UCSC Ensembl
Innerchr11:42908857..42929829hg18UCSC Ensembl
Innerchr11:42908857..42929829hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3820973
hg1920973
hg1820973
hg1720973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694147
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522240
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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