A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585720



Internal ID20958791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78788371..78789834hg38UCSC Ensembl
chr13:79362506..79363969hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381464
hg191464
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233418
Samples
Known GenesLINC00331
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585720
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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