A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576559



Internal ID20949630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:185241..186599hg38UCSC Ensembl
chr18:185241..186599hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg381359
hg191359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244127
Samples
Known GenesUSP14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576559
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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