A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042528



Internal ID19131747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20396289..20746114hg38UCSC Ensembl
Innerchr15:20601542..20951443hg19UCSC Ensembl
Innerchr15:18861556..19211451hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38349826
hg19349902
hg18349896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2257n100
Supporting Variantsnssv3539662
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042528
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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