A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547837



Internal ID18499432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32247324..32623392hg38UCSC Ensembl
Innerchr15:32539525..32915593hg19UCSC Ensembl
Innerchr15:30326817..30702885hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38376069
hg19376069
hg18376069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038003
Supporting Variants
Samples
Known GenesARHGAP11A, GOLGA8K, GOLGA8O, GOLGA8R, 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)nssv3547837
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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