A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588991



Internal ID16376400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37352354..37353573hg38UCSC Ensembl
Innerchr22:37748394..37749613hg19UCSC Ensembl
Innerchr22:36078340..36079559hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381220
hg191220
hg181220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8101n54
Supporting Variantsnssv956665
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588991
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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