A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010887



Internal ID21920230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:99042734..99047910hg38UCSC Ensembl
chr8:100054962..100060138hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg385177
hg195177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595134
Samples
Known GenesVPS13B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010887
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