A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588871



Internal ID16376280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26967361..26985173hg38UCSC Ensembl
Innerchr22:27363324..27381136hg19UCSC Ensembl
Innerchr22:25693324..25711136hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3817813
hg1917813
hg1817813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151731
SamplesHGDP00532
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588871
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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