A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258435



Internal ID20825475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79635233..79635699hg38UCSC Ensembl
chr2:79862359..79862825hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538914
Supporting Variants
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258435
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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