A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3539661



Internal ID18837942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20396289..20670977hg38UCSC Ensembl
Innerchr15:20601542..20876306hg19UCSC Ensembl
Innerchr15:18861556..19136320hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38274689
hg19274765
hg18274765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053484
Supporting Variants
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)nssv3539661
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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