A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3588878



Internal ID18540473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21977669..22114208hg38UCSC Ensembl
Innerchr22:22332041..22468619hg19UCSC Ensembl
Innerchr22:20662041..20798619hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38136540
hg19136579
hg18136579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056665
Supporting Variants
Samples
Known GenesTOP3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3588878
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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