A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647612



Internal ID6687666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33062982..33075332hg38UCSC Ensembl
Innerchr22:33063001..33075313hg38UCSC Ensembl
Outerchr22:33062963..33075351hg38UCSC Ensembl
chr22:33458968..33471318hg19UCSC Ensembl
Innerchr22:33458987..33471299hg19UCSC Ensembl
Outerchr22:33458949..33471337hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3812351
hg1912351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16405310
SamplesHG00362
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647612
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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