A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568836



Internal ID16356245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31727716..32223772hg38UCSC Ensembl
Innerchr15:32019919..32515973hg19UCSC Ensembl
Innerchr15:29807211..30303265hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38496057
hg19496055
hg18496055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4440n54
Supporting Variantsnssv839671, nssv839670, nssv839673, nssv839672, nssv839674
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568836
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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