A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588897



Internal ID16376306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:32720328..32743244hg38UCSC Ensembl
Innerchr22:33116314..33139230hg19UCSC Ensembl
Innerchr22:31446314..31469230hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3822917
hg1922917
hg1822917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954614
Samples
Known GenesSYN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588897
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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