A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046257



Internal ID19135476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101390109..101530416hg38UCSC Ensembl
Innerchr15:101930314..102070619hg19UCSC Ensembl
Innerchr15:99747837..99888142hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38140308
hg19140306
hg18140306
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2674n100
Supporting Variantsnssv3555342
Samples
Known GenesPCSK6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046257
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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