A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568827



Internal ID16356236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31713041..32178810hg38UCSC Ensembl
Innerchr15:32005244..32471011hg19UCSC Ensembl
Innerchr15:29792536..30258303hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38465770
hg19465768
hg18465768
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4440n54
Supporting Variantsnssv839659
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568827
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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