A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231784



Internal ID20798824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119002225..119002393hg38UCSC Ensembl
chr11:118872935..118873103hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592315
Supporting Variants
Samples
Known GenesCCDC84
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231784
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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