A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450549



Internal ID228752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79635409..79636186hg38UCSC Ensembl
chr2:79862535..79863312hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38778
hg19778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16915767
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450549
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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