A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072991



Internal ID20640031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21595241..21595563hg38UCSC Ensembl
chr22:21949530..21949852hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554706
Supporting Variants
Samples
Known GenesUBE2L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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