A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069151



Internal ID21978384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30889934..30889934hg38UCSC Ensembl
chr8:30747450..30747450hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069151
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