A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582758



Internal ID20955829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:184610..185144hg38UCSC Ensembl
chr18:184610..185144hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38535
hg19535
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244126
Samples
Known GenesUSP14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582758
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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