A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163933



Internal ID20730973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121952948..121960821hg38UCSC Ensembl
chr8:122965187..122973060hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg387874
hg197874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425229
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163933
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