A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567274



Internal ID16354683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20207597..20996787hg38UCSC Ensembl
Innerchr15:20412850..21202116hg19UCSC Ensembl
Innerchr15:18672864..19466775hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38789191
hg19789267
hg18793912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4166n54
Supporting Variantsnssv837042, nssv837043, nssv837044
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567274
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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