A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246799



Internal ID20813839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24185346..24186046hg38UCSC Ensembl
chr18:21765310..21766010hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589747
Supporting Variants
Samples
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246799
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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