A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204565



Internal ID20771605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32531901..32532600hg38UCSC Ensembl
chr22:32927888..32928587hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547339
Supporting Variants
Samples
Known GenesSYN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204565
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.66756


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