A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275882



Internal ID20485100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10458873..10458873hg38UCSC Ensembl
chr5:10458985..10458985hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753320
Supporting Variants
Samples
Known GenesROPN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275882
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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