A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244059



Internal ID20811099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32025665..32026101hg38UCSC Ensembl
chr18:29605628..29606064hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589110
Supporting Variants
Samples
Known GenesRNF125
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244059
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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