A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647667



Internal ID7034407
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16413112, essv16413113, essv16413111, essv16413110
SamplesNA12843, NA11992, HG00328, HG02051
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647667
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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