A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547839



Internal ID18499434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32257489..32497505hg38UCSC Ensembl
Innerchr15:32549690..32789706hg19UCSC Ensembl
Innerchr15:30336982..30576998hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38240017
hg19240017
hg18240017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049139
Supporting Variants
Samples
Known GenesGOLGA8K, GOLGA8O, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3547839
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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