A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581143



Internal ID20954214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116797489..116798225hg38UCSC Ensembl
chr11:116668205..116668941hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228195
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581143
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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