A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010571



Internal ID19099788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179159177..179170365hg38UCSC Ensembl
Innerchr3:178876965..178888153hg19UCSC Ensembl
Innerchr3:180359659..180370847hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3811189
hg1911189
hg1811189
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614988
Samples
Known GenesPIK3CA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010571
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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