A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754494



Internal ID20530354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50165996..50165996hg38UCSC Ensembl
chr22:50604425..50604425hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754494
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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