A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592418



Internal ID21784461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106285864..106285864hg38UCSC Ensembl
chr8:107298092..107298092hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079065
Supporting Variants
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592418
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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