A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054317



Internal ID21963550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26671407..26671407hg38UCSC Ensembl
chr3:26712898..26712898hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550574
Samples
Known GenesLRRC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054317
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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