A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050335



Internal ID21959568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80075590..80075590hg38UCSC Ensembl
chr2:80302716..80302716hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518318
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050335
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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