A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041366



Internal ID19130585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20210878..22145275hg38UCSC Ensembl
Innerchr15:20416131..22433226hg19UCSC Ensembl
Innerchr15:18676145..19934590hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381934398
hg192017096
hg181258446
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2214n100
Supporting Variantsnssv3538222
Samples
Known GenesCHEK2P2, CT60, 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)nsv1041366
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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