A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526036



Internal ID15106643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2764393..2767686hg38UCSC Ensembl
Innerchr11:2785623..2788916hg19UCSC Ensembl
Innerchr11:2742199..2745492hg18UCSC Ensembl
Innerchr11:2742199..2745492hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg383294
hg193294
hg183294
hg173294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702267
Samples
Known GenesKCNQ1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526036
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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