A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527620



Internal ID15108227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106795333..106795607hg38UCSC Ensembl
Innerchr11:106666059..106666333hg19UCSC Ensembl
Innerchr11:106171269..106171543hg18UCSC Ensembl
Innerchr11:106171269..106171543hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38275
hg19275
hg18275
hg17275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704086
Samples
Known GenesGUCY1A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527620
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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