A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568863



Internal ID16356272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32151995..32219354hg38UCSC Ensembl
Innerchr15:32444196..32511555hg19UCSC Ensembl
Innerchr15:30231488..30298847hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3867360
hg1967360
hg1867360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839712
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568863
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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