A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294784



Internal ID20504002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36126349..36126349hg38UCSC Ensembl
chr22:36522397..36522397hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766681
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294784
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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