A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586856



Internal ID20959927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126108535..126109297hg38UCSC Ensembl
chr11:125978430..125979192hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230676
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586856
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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