A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595807



Internal ID20968878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69530621..70010332hg38UCSC Ensembl
chr18:67197857..67677568hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38479712
hg19479712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244736
Samples
Known GenesCD226, DOK6, RTTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595807
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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