A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272138



Internal ID20839178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90593406..90594571hg38UCSC Ensembl
chr6:91303125..91304290hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272138
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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