A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614307



Internal ID21806354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116780154..116780272hg38UCSC Ensembl
chr11:116650870..116650988hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040349
Supporting Variants
Samples
Known GenesZNF259
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614307
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