A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066259



Internal ID21975492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33892826..33892826hg38UCSC Ensembl
chr3:33934318..33934318hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552139
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066259
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