A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16413111



Internal ID2296211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35628099..35630909hg38UCSC Ensembl
Innerchr22:35628104..35630904hg38UCSC Ensembl
Outerchr22:35628094..35630914hg38UCSC Ensembl
chr22:36024146..36026956hg19UCSC Ensembl
Innerchr22:36024151..36026951hg19UCSC Ensembl
Outerchr22:36024141..36026961hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647667
Supporting Variants
SamplesHG02051
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16413111
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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