A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050158



Internal ID19139377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57363578..57486837hg38UCSC Ensembl
Innerchr15:57655776..57779035hg19UCSC Ensembl
Innerchr15:55443068..55566327hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38123260
hg19123260
hg18123260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2607n100
Supporting Variantsnssv3553607
Samples
Known GenesCGNL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050158
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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