A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588119



Internal ID16028842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:17937289..17966194hg38UCSC Ensembl
Innerchr22:18420055..18448960hg19UCSC Ensembl
Innerchr22:16800055..16828960hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3828906
hg1928906
hg1828906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv951503
Samples
Known GenesMICAL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588119
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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