A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761642



Internal ID20537502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35389370..35389370hg38UCSC Ensembl
chr22:35785363..35785363hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276209
Samples
Known GenesHMOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761642
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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