A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520109



Internal ID21844468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80494682..80494682hg38UCSC Ensembl
chr2:80721807..80721807hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042203
Supporting Variants
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520109
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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