A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266088



Internal ID20475306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3261762..3261762hg38UCSC Ensembl
chr20:3242408..3242408hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758064
Supporting Variants
Samples
Known GenesC20orf194
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266088
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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