A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3537275



Internal ID18835556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20988783hg38UCSC Ensembl
Innerchr15:20585976..21194112hg19UCSC Ensembl
Innerchr15:18845990..19458771hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38608061
hg19608137
hg18612782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053081
Supporting Variants
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3537275
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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