A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590698



Internal ID20963769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38631545..38633890hg38UCSC Ensembl
chr11:38653095..38655440hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382346
hg192346
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225054
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590698
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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