A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17017950



Internal ID79617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116273272..116293241hg38UCSC Ensembl
chr8:117285505..117305476hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3819970
hg1919972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486485
Supporting Variants
Samples
Known GenesLINC00536
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17017950
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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