A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044892



Internal ID19134111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..20689298hg38UCSC Ensembl
Innerchr15:20564575..20894627hg19UCSC Ensembl
Innerchr15:18824589..19172949hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38329977
hg19330053
hg18348361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2228n100
Supporting Variantsnssv3537560
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)nsv1044892
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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