A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172859



Internal ID20739899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92352068..92352858hg38UCSC Ensembl
chr8:93364296..93365086hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425700
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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