A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593428



Internal ID20966499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58992185..58992763hg38UCSC Ensembl
chr15:59284384..59284962hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241187
Samples
Known GenesRNF111
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593428
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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