A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893442



Internal ID19184262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21071480..21109441hg38UCSC Ensembl
Outerchr22:21071480..21109441hg38UCSC Ensembl
Innerchr22:21425769..21463730hg19UCSC Ensembl
Outerchr22:21425769..21463730hg19UCSC Ensembl
Innerchr22:19755769..19793730hg18UCSC Ensembl
Outerchr22:19755769..19793730hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3837962
hg1937962
hg1837962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788311
Samples
Known GenesBCRP2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893442
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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