A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040963



Internal ID19130182
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 StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3714797
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)nsv1040963
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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