A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588939



Internal ID16376348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:34421035..34462627hg38UCSC Ensembl
Innerchr22:34817025..34858619hg19UCSC Ensembl
Innerchr22:33147025..33188619hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3841593
hg1941595
hg1841595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954745
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588939
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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