A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274033



Internal ID20483251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17330638..17330638hg38UCSC Ensembl
chr22:17811528..17811528hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274033
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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