A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5469648



Internal ID8876018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35628098..35630898hg38UCSC Ensembl
chr22:36024145..36026945hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382801
hg192801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673489
Supporting Variants
SamplesHG00328
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5469648
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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