A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599364



Internal ID20972435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3982063..3982560hg38UCSC Ensembl
chr20:3962710..3963207hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251418
Samples
Known GenesRNF24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599364
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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