A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204511



Internal ID20771551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17558792..17582143hg38UCSC Ensembl
chr22:18038493..18064909hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3823352
hg1926417
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553953
Supporting Variants
Samples
Known GenesSLC25A18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204511
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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