A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525453



Internal ID15106060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2764393..2765831hg38UCSC Ensembl
Innerchr11:2785623..2787061hg19UCSC Ensembl
Innerchr11:2742199..2743637hg18UCSC Ensembl
Innerchr11:2742199..2743637hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381439
hg191439
hg181439
hg171439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701581
Samples
Known GenesKCNQ1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525453
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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