A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6277496



Internal ID9183861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17289460..17298218hg38UCSC Ensembl
chr22:17770350..17779108hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg388759
hg198759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666737
Supporting Variants
SamplesHG01441
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6277496
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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