A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108331



Internal ID22017564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31679606..31679606hg38UCSC Ensembl
chr22:32075592..32075592hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108331
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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