A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588057



Internal ID16375466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:16375777..16386765hg38UCSC Ensembl
Innerchr22:16856439..16867427hg19UCSC Ensembl
Innerchr22:15236439..15247427hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3810989
hg1910989
hg1810989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7945n54
Supporting Variantsnssv949489
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588057
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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