A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204627



Internal ID20771667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37336447..37367394hg38UCSC Ensembl
chr22:37732488..37763434hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3830948
hg1930947
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542536
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204627
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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