A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3648066



Internal ID7034803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49637455..49654021hg38UCSC Ensembl
Innerchr22:49637955..49653521hg38UCSC Ensembl
Outerchr22:49636455..49655021hg38UCSC Ensembl
chr22:50031103..50047669hg19UCSC Ensembl
Innerchr22:50031603..50047169hg19UCSC Ensembl
Outerchr22:50030103..50048669hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3816567
hg1916567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16457742
SamplesHG02477
Known GenesC22orf34
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3648066
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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