A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173767



Internal ID20740807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95968751..95969194hg38UCSC Ensembl
chr8:96980979..96981422hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429493
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00066


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