A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221413



Internal ID20788453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66165805..66166499hg38UCSC Ensembl
chr10:67925563..67926257hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588399
Supporting Variants
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221413
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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