A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258444



Internal ID20825484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80231750..80234415hg38UCSC Ensembl
chr2:80458875..80461540hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg382666
hg192666
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554828
Supporting Variants
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258444
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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