A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583092



Internal ID20956163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24197359..24197793hg38UCSC Ensembl
chr18:21777323..21777757hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246800
Samples
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583092
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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