A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091091



Internal ID20658131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80524437..80524854hg38UCSC Ensembl
chr2:80751562..80751979hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354510
Supporting Variants
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00057


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