A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223888



Internal ID20790928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10094185..10094814hg38UCSC Ensembl
chr11:10115732..10116361hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576001
Supporting Variants
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223888
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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