A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448800



Internal ID22506670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97550096..97555045hg38UCSC Ensembl
chr8:98562324..98567273hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg384950
hg194950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918834
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448800
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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