A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595593



Internal ID21787636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97612339..97615093hg38UCSC Ensembl
chr8:98624567..98627321hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382755
hg192755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595593
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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