A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588919



Internal ID16029642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33384911..33386022hg38UCSC Ensembl
Innerchr22:33780897..33782008hg19UCSC Ensembl
Innerchr22:32110897..32112008hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381112
hg191112
hg181112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954685, nssv954686, nssv954684
Samples
Known GenesLARGE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588919
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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