A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523559



Internal ID15104166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125302697..125302778hg38UCSC Ensembl
Innerchr11:125172593..125172674hg19UCSC Ensembl
Innerchr11:124677803..124677884hg18UCSC Ensembl
Innerchr11:124677803..124677884hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3882
hg1982
hg1882
hg1782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699339
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523559
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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