A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756200



Internal ID20532060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34034615..34034615hg38UCSC Ensembl
chr22:34430604..34430604hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756200
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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