A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915767



Internal ID11244
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 StatusS
Merged Variantsnsv5450549
Supporting Variants
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915767
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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