A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586166



Internal ID20959237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73089006..73089633hg38UCSC Ensembl
chr14:73555714..73556341hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238638
Samples
Known GenesRBM25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586166
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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