A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv954398



Internal ID15901668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25268441..25513237hg38UCSC Ensembl
Innerchr22:25664408..25909204hg19UCSC Ensembl
Innerchr22:23994408..24239204hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38244797
hg19244797
hg18244797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588794
Supporting Variants
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)nssv954398
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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