A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999990



Internal ID7082598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:16367222..16375354hg38UCSC Ensembl
Innerchr22:16847884..16856016hg19UCSC Ensembl
Innerchr22:15227884..15236016hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg388133
hg198133
hg188133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586490
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999990
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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