A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040584



Internal ID19129803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20396289..22194283hg38UCSC Ensembl
Innerchr15:20601542..22482234hg19UCSC Ensembl
Innerchr15:18861556..19983598hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381797995
hg191880693
hg181122043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3539694
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)nsv1040584
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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