A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519454



Internal ID15446747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6314332..6333786hg38UCSC Ensembl
Innerchr11:6335562..6355016hg19UCSC Ensembl
Innerchr11:6292138..6311592hg18UCSC Ensembl
Innerchr11:6292138..6311592hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3819455
hg1919455
hg1819455
hg1719455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696862
Samples
Known GenesPRKCDBP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519454
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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