A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011392



Internal ID21920735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80232387..80232502hg38UCSC Ensembl
chr8:81144622..81144737hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586443
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011392
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