A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768299



Internal ID20544159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27051910..27051910hg38UCSC Ensembl
chr22:27447872..27447872hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283555
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768299
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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