A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063952



Internal ID19153171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42041983..42138636hg38UCSC Ensembl
Innerchr18:39621947..39718600hg19UCSC Ensembl
Innerchr18:37875945..37972598hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3896654
hg1996654
hg1896654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3342n100
Supporting Variantsnssv3565347
Samples
Known GenesPIK3C3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063952
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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