A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292079



Internal ID20501297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17369342..17369342hg38UCSC Ensembl
chr22:17850241..17850241hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38923
hg19923
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753738
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292079
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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