A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039393



Internal ID18781924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101395007..101733297hg38UCSC Ensembl
Innerchr15:101935212..102273500hg19UCSC Ensembl
Innerchr15:99752735..100091023hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38338291
hg19338289
hg18338289
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2675n100
Supporting Variantsnssv3555343
Samples
Known GenesPCSK6, TARSL2, TM2D3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039393
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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