A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222530



Internal ID20789570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59825896..59827200hg38UCSC Ensembl
chr11:59593369..59594673hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381305
hg191305
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589142
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222530
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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