A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528959



Internal ID15109566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17382092..17413667hg38UCSC Ensembl
Innerchr11:17403639..17435214hg19UCSC Ensembl
Innerchr11:17360215..17391790hg18UCSC Ensembl
Innerchr11:17360215..17391790hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3831576
hg1931576
hg1831576
hg1731576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv59n21
Supporting Variantsnssv705655
Samples
Known GenesABCC8, KCNJ11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528959
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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