A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524471



Internal ID15451764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179179886..179185476hg38UCSC Ensembl
Innerchr3:178897674..178903264hg19UCSC Ensembl
Innerchr3:180380368..180385958hg18UCSC Ensembl
Innerchr3:180380376..180385966hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg385591
hg195591
hg185591
hg175591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700409
Samples
Known GenesPIK3CA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524471
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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