A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989856



Internal ID21899199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79768339..79768514hg38UCSC Ensembl
chr2:79995465..79995640hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531858
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989856
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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