A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589058



Internal ID20962129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116395432..116395891hg38UCSC Ensembl
chr11:116266149..116266608hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589058
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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