A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567270



Internal ID16354679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20207597..20956011hg38UCSC Ensembl
Innerchr15:20412850..21161340hg19UCSC Ensembl
Innerchr15:18672864..19425999hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38748415
hg19748491
hg18753136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4166n54
Supporting Variantsnssv837038
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)nsv567270
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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