A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236513



Internal ID20803553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47462840..47463228hg38UCSC Ensembl
chr11:47484392..47484780hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582117
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236513
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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