A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877201



Internal ID22652164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21566153..21607239hg38UCSC Ensembl
chr22:21920442..21961528hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3841087
hg1941087
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489494
Samples
Known GenesUBE2L3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877201
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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