A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050278



Internal ID19139497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20364686..22095238hg38UCSC Ensembl
Innerchr15:20569939..22383189hg19UCSC Ensembl
Innerchr15:18829953..19884553hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381730553
hg191813251
hg181054601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3535792
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, 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)nsv1050278
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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