A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052049



Internal ID21961282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80577687..80577687hg38UCSC Ensembl
chr2:80804812..80804812hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517856
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052049
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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