A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568833



Internal ID16356242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31726528..32222725hg38UCSC Ensembl
Innerchr15:32018731..32514926hg19UCSC Ensembl
Innerchr15:29806023..30302218hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38496198
hg19496196
hg18496196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4440n54
Supporting Variantsnssv839668
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568833
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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