A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586011



Internal ID20959082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54577958..54578860hg38UCSC Ensembl
chr18:52245189..52246091hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3373n223
Supporting Variantsnssv18244681
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586011
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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