A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593413



Internal ID20966484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33516296..33517564hg38UCSC Ensembl
chr18:31096260..31097528hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381269
hg191269
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244162
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593413
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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