A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220402



Internal ID20787442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96399529..96399878hg38UCSC Ensembl
chr11:96132693..96133042hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587867
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220402
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.01319


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