A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765753



Internal ID20541613
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 StatusM
Merged Variants
Supporting Variantsnssv16290455
Samples
Known GenesCBLB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765753
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer