A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568848



Internal ID16356257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31804319..32128207hg38UCSC Ensembl
Innerchr15:32096522..32420408hg19UCSC Ensembl
Innerchr15:29883814..30207700hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38323889
hg19323887
hg18323887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4442n54
Supporting Variantsnssv839689
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568848
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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