A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659066



Internal ID15049032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17386478..17406315hg38UCSC Ensembl
Innerchr11:17408025..17427862hg19UCSC Ensembl
Innerchr11:17364601..17384438hg18UCSC Ensembl
Innerchr11:17364601..17384438hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3819838
hg1919838
hg1819838
hg1719838
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517772
Supporting Variants
Samples
Known GenesABCC8, KCNJ11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659066
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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