A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206684



Internal ID20773724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21598775..21609001hg38UCSC Ensembl
chr22:21953064..21963290hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3810227
hg1910227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550229
Supporting Variants
Samples
Known GenesUBE2L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206684
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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