A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272095



Internal ID20839135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89078135..89078646hg38UCSC Ensembl
chr6:89787854..89788365hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558222
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272095
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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