A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226734



Internal ID20793774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89901801..89903300hg38UCSC Ensembl
chr8:90914029..90915528hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416993
Supporting Variants
Samples
Known GenesOSGIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226734
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00011


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