A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044667



Internal ID19133886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..20752649hg38UCSC Ensembl
Innerchr15:20564575..20957978hg19UCSC Ensembl
Innerchr15:18824589..19217991hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38393328
hg19393404
hg18393403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2228n100
Supporting Variantsnssv3537566
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)nsv1044667
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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