A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3546466



Internal ID18498061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30094196..30795118hg38UCSC Ensembl
Innerchr15:30386399..31087321hg19UCSC Ensembl
Innerchr15:28173691..28874613hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38700923
hg19700923
hg18700923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049639
Supporting Variants
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC100288637, LOC101059918, 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)nssv3546466
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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