A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893435



Internal ID18837569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20230714..20307897hg38UCSC Ensembl
Outerchr22:20230714..20307897hg38UCSC Ensembl
Innerchr22:20218237..20295420hg19UCSC Ensembl
Outerchr22:20218237..20295420hg19UCSC Ensembl
Innerchr22:18598237..18675420hg18UCSC Ensembl
Outerchr22:18598237..18675420hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3877184
hg1977184
hg1877184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789526
Samples
Known GenesMIR1286, RTN4R
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893435
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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