A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5923916



Internal ID8776336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23234669..23235625hg38UCSC Ensembl
chr22:23576856..23577812hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665954
Supporting Variants
SamplesHG00178
Known GenesBCR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5923916
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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