A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167111



Internal ID20734151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23051601..23059400hg38UCSC Ensembl
chr8:22909114..22916913hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429426
Supporting Variants
Samples
Known GenesTNFRSF10B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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