A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279761



Internal ID20488979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206943688..206943688hg38UCSC Ensembl
chr2:207808412..207808412hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754610
Supporting Variants
Samples
Known GenesCPO
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279761
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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