A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671523



Internal ID9937628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25218236..25218826hg38UCSC Ensembl
chr22:25614203..25614793hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5765823, essv6552851, essv6011226, essv5446431
SamplesNA10851, HG00281, HG00268, HG00282
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671523
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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