A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797513



Internal ID18834610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:18905062..19020595hg38UCSC Ensembl
Innerchr22:18892575..19008108hg19UCSC Ensembl
Innerchr22:17272575..17388108hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38115534
hg19115534
hg18115534
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893431
Supporting Variants
Samples
Known GenesDGCR5, DGCR6, DGCR9, PRODH
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=42
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797513
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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