A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586279



Internal ID20959350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24865982..25342771hg38UCSC Ensembl
chr18:22445946..22922735hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38476790
hg19476790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246828
Samples
Known GenesZNF521
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586279
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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