A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568859



Internal ID16356268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31870989..32240135hg38UCSC Ensembl
Innerchr15:32163192..32532336hg19UCSC Ensembl
Innerchr15:29950484..30319628hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38369147
hg19369145
hg18369145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4444n54
Supporting Variantsnssv839711
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568859
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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