A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245519



Internal ID20812559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:66531656..66531987hg38UCSC Ensembl
chr18:64198893..64199224hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599694
Supporting Variants
Samples
Known GenesCDH19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245519
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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