A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589115



Internal ID20962186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116914541..116915656hg38UCSC Ensembl
chr12:117352346..117353461hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg381116
hg191116
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226754
Samples
Known GenesFBXW8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589115
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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