A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588099



Internal ID16028822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:17333921..17436386hg38UCSC Ensembl
Innerchr22:17814811..17915430hg19UCSC Ensembl
Innerchr22:16194811..16295430hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38102466
hg19100620
hg18100620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152422
SamplesNINDS_173
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588099
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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