A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568832



Internal ID16356241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31726528..32222140hg38UCSC Ensembl
Innerchr15:32018731..32514341hg19UCSC Ensembl
Innerchr15:29806023..30301633hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38495613
hg19495611
hg18495611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4440n54
Supporting Variantsnssv839667
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568832
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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