A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555129



Internal ID21879484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169962273..169962273hg38UCSC Ensembl
chr3:169680061..169680061hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061106
Supporting Variants
Samples
Known GenesLOC100128164
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555129
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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