A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273942



Internal ID20840982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65479942..67131267hg38UCSC Ensembl
chr6:66189835..67841160hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381651326
hg191651326
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558425
Supporting Variants
Samples
Known GenesEYS, SLC25A51P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273942
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00041


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