A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284917



Internal ID20494135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69611298..69611298hg38UCSC Ensembl
chr4:70477016..70477016hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756015
Supporting Variants
Samples
Known GenesUGT2A1, UGT2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284917
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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