A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036233



Internal ID19125452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376297..20688370hg38UCSC Ensembl
Innerchr15:20581550..20893699hg19UCSC Ensembl
Innerchr15:18841564..19153713hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38312074
hg19312150
hg18312150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2228n100
Supporting Variantsnssv3535951
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036233
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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