A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162986



Internal ID20730028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106728301..106730100hg38UCSC Ensembl
chr8:107740529..107742328hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429141
Supporting Variants
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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