A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584462



Internal ID20957533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33528198..33536872hg38UCSC Ensembl
chr18:31108162..31116836hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg388675
hg198675
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584462
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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