A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588237



Internal ID20961308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33598232..33598317hg38UCSC Ensembl
chr15:33890433..33890518hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239518
Samples
Known GenesRYR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588237
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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