A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583959



Internal ID20957030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113550763..113553099hg38UCSC Ensembl
chr11:113421485..113423821hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg382337
hg192337
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217237
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583959
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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