A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588884



Internal ID16029607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:30098382..30194037hg38UCSC Ensembl
Innerchr22:30494371..30590026hg19UCSC Ensembl
Innerchr22:28824371..28920026hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3895656
hg1995656
hg1895656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954558
Samples
Known GenesHORMAD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588884
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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