A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669903



Internal ID9936008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:29591763..29602202hg38UCSC Ensembl
Outerchr22:29591726..29602252hg38UCSC Ensembl
Innerchr22:29987752..29998191hg19UCSC Ensembl
Outerchr22:29987715..29998241hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3810527
hg1910527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5600823
SamplesHG00261
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669903
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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