A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594928



Internal ID20967999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42829111..42830442hg38UCSC Ensembl
chr18:40409076..40410407hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg381332
hg191332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244919
Samples
Known GenesRIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594928
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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