A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170033



Internal ID21314094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179149798..179160372hg38UCSC Ensembl
Outerchr3:179146357..179165384hg38UCSC Ensembl
Innerchr3:178867586..178878160hg19UCSC Ensembl
Outerchr3:178864145..178883172hg19UCSC Ensembl
Innerchr3:180350280..180360854hg18UCSC Ensembl
Outerchr3:180346839..180365866hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3819028
hg1919028
hg1819028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241288
SamplesNGO_32
Known GenesPIK3CA
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170033
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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