A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204664



Internal ID20771704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39024906..39044821hg38UCSC Ensembl
chr22:39420911..39440826hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3819916
hg1919916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536952
Supporting Variants
Samples
Known GenesAPOBEC3D, APOBEC3F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204664
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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