A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290455



Internal ID20499673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105663063..105663063hg38UCSC Ensembl
chr3:105381907..105381907hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765753
Supporting Variants
Samples
Known GenesCBLB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290455
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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