A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244131



Internal ID20811171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21531732..21533545hg38UCSC Ensembl
chr18:19111693..19113506hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381814
hg191814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588289
Supporting Variants
Samples
Known GenesESCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244131
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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