A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589329



Internal ID20962400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59045097..59045833hg38UCSC Ensembl
chr18:56712329..56713065hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245386
Samples
Known GenesOACYLP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589329
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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