A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589396



Internal ID20962467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62466457..62467189hg38UCSC Ensembl
chr18:60133690..60134422hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589396
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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