A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290750



Internal ID20499968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73315155..73315155hg38UCSC Ensembl
chr8:74227390..74227390hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766106
Supporting Variants
Samples
Known GenesRDH10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290750
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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