A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594759



Internal ID20967830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35699173..35707498hg38UCSC Ensembl
chr11:35720721..35729046hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg388326
hg198326
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219650
Samples
Known GenesTRIM44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594759
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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