A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568857



Internal ID16356266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31870926..32223772hg38UCSC Ensembl
Innerchr15:32163129..32515973hg19UCSC Ensembl
Innerchr15:29950421..30303265hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38352847
hg19352845
hg18352845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4444n54
Supporting Variantsnssv839709
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568857
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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