A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226260



Internal ID20793300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35129593..35130442hg38UCSC Ensembl
chr11:35151140..35151989hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593187
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226260
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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