A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592951



Internal ID20966022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18503371..18503938hg38UCSC Ensembl
chr11:18524918..18525485hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235297
Samples
Known GenesTSG101
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592951
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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