A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3614988



Internal ID18913269
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 StatusS
Merged Variantsnsv1010571
Supporting Variants
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)nssv3614988
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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