A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264787



Internal ID20474005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53226631..53226631hg38UCSC Ensembl
chr8:54139191..54139191hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757397
Supporting Variants
Samples
Known GenesOPRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264787
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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