A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230966



Internal ID20798006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69150596..69150988hg38UCSC Ensembl
chr10:70910352..70910744hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575803
Supporting Variants
Samples
Known GenesVPS26A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230966
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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