A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223645



Internal ID20790685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116769808..116770730hg38UCSC Ensembl
chr11:116640524..116641446hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38923
hg19923
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587577
Supporting Variants
Samples
Known GenesBUD13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223645
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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