A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588244



Internal ID16028967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20042355..20072240hg38UCSC Ensembl
Innerchr22:20029878..20059763hg19UCSC Ensembl
Innerchr22:18409878..18439763hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3829886
hg1929886
hg1829886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7985n54
Supporting Variantsnssv951876, nssv951875
Samples
Known GenesTANGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588244
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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