A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528154



Internal ID21852511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200760871..200760871hg38UCSC Ensembl
chr2:201625594..201625594hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046458
Supporting Variants
Samples
Known GenesAOX2P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528154
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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