A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489494



Internal ID22547413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21566153..21607239hg38UCSC Ensembl
chr22:21920442..21961528hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3841087
hg1941087
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877201
Supporting Variants
Samples
Known GenesUBE2L3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489494
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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