A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222204



Internal ID20789244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92393793..92440895hg38UCSC Ensembl
chr8:93406021..93453123hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3847103
hg1947103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432698
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222204
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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