A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204666



Internal ID20771706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39033918..39052771hg38UCSC Ensembl
chr22:39429923..39448776hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3818854
hg1918854
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540034
Supporting Variants
Samples
Known GenesAPOBEC3F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204666
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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