A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241886



Internal ID20808926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72517478..72518506hg38UCSC Ensembl
chr15:72809819..72810847hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381029
hg191029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580241
Supporting Variants
Samples
Known GenesARIH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241886
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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