A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3614987



Internal ID18566582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179158015..179168505hg38UCSC Ensembl
Innerchr3:178875803..178886293hg19UCSC Ensembl
Innerchr3:180358497..180368987hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3810491
hg1910491
hg1810491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003540
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)nssv3614987
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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