A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519052



Internal ID15446345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8432047..8453337hg38UCSC Ensembl
Innerchr11:8453594..8474884hg19UCSC Ensembl
Innerchr11:8410170..8431460hg18UCSC Ensembl
Innerchr11:8410170..8431460hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3821291
hg1921291
hg1821291
hg1721291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696523
Samples
Known GenesSTK33
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519052
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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