A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025534



Internal ID21934877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79107160..79107310hg38UCSC Ensembl
chr16:79141057..79141207hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618825
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025534
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