A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594665



Internal ID21786708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53226627..53226627hg38UCSC Ensembl
chr8:54139187..54139187hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064700
Supporting Variants
Samples
Known GenesOPRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594665
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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