A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714797



Internal ID19013078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20396289..22182059hg38UCSC Ensembl
Innerchr15:20601542..22470010hg19UCSC Ensembl
Innerchr15:18861556..19971374hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381785771
hg191868469
hg181109819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040963
Supporting Variants
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, 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)nssv3714797
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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