A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741477



Internal ID20517454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19551261..19551343hg38UCSC Ensembl
chr22:19538784..19538866hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741477
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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