A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219497



Internal ID20786537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8620254..8620857hg38UCSC Ensembl
chr11:8641801..8642404hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587253
Supporting Variants
Samples
Known GenesTRIM66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219497
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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