A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721640



Internal ID18673235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32219037..32584771hg38UCSC Ensembl
Innerchr15:32511238..32876972hg19UCSC Ensembl
Innerchr15:30298530..30664264hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38365735
hg19365735
hg18365735
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045730
Supporting Variants
Samples
Known GenesGOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3721640
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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