A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039501



Internal ID19128720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376186..20609659hg38UCSC Ensembl
Innerchr15:20581439..20814965hg19UCSC Ensembl
Innerchr15:18841453..19074979hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38233474
hg19233527
hg18233527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2236n100
Supporting Variantsnssv3535888
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039501
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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