A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660524



Internal ID9579943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37736681..37741331hg38UCSC Ensembl
chr22:38132688..38137338hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg384651
hg194651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6427501, essv5425482
SamplesNA19703, NA19704
Known GenesTRIOBP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660524
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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