A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111880



Internal ID22021114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32331007..32331007hg38UCSC Ensembl
chr22:32726994..32726994hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111880
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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