A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173093



Internal ID20740133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8996652..8998895hg38UCSC Ensembl
chr8:8854162..8856405hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382244
hg192244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422618
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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