A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762943



Internal ID20538803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48306026..48306026hg38UCSC Ensembl
chr22:48701838..48701838hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762943
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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