A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647984



Internal ID7034723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47372622..47382221hg38UCSC Ensembl
Innerchr22:47372637..47382206hg38UCSC Ensembl
Outerchr22:47372607..47382236hg38UCSC Ensembl
chr22:47768372..47777971hg19UCSC Ensembl
Innerchr22:47768387..47777956hg19UCSC Ensembl
Outerchr22:47768357..47777986hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16448584
SamplesHG03720
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647984
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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