A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107726



Internal ID22016959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33132512..33132512hg38UCSC Ensembl
chr22:33528498..33528498hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107726
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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