A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272115



Internal ID20839155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89775894..89776201hg38UCSC Ensembl
chr6:90485613..90485920hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563821
Supporting Variants
Samples
Known GenesMDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272115
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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