A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588830



Internal ID16376239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25303640..25528477hg38UCSC Ensembl
Innerchr22:25699607..25924444hg19UCSC Ensembl
Innerchr22:24029607..24254444hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38224838
hg19224838
hg18224838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8075n54
Supporting Variantsnssv954515
Samples
Known GenesCRYBB2P1, IGLL3P, LRP5L, MIR6817
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588830
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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