A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236290



Internal ID20803330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47736432..47737524hg38UCSC Ensembl
chr11:47757984..47759076hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381093
hg191093
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591503
Supporting Variants
Samples
Known GenesFNBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236290
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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