A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561648



Internal ID334619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8445866..8493577hg38UCSC Ensembl
chr11:8467413..8515124hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3847712
hg1947712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041859
Samples
Known GenesSTK33
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561648
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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