A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014808



Internal ID21924151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54480319..54480376hg38UCSC Ensembl
chr8:55392879..55392936hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587279
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014808
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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