A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893464



Internal ID18837598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:24683958..24728744hg38UCSC Ensembl
Outerchr22:24683958..24728744hg38UCSC Ensembl
Innerchr22:25079925..25124711hg19UCSC Ensembl
Outerchr22:25079925..25124711hg19UCSC Ensembl
Innerchr22:23409925..23454711hg18UCSC Ensembl
Outerchr22:23409925..23454711hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3844787
hg1944787
hg1844787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787851
Samples
Known GenesPIWIL3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893464
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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