A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224076



Internal ID20791116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109051472..109169483hg38UCSC Ensembl
chr8:110063701..110181712hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38118012
hg19118012
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421751
Supporting Variants
Samples
Known GenesTRHR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224076
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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