A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559355



Internal ID332391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18248810..18266106hg38UCSC Ensembl
chr11:18270357..18287653hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3817297
hg1917297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv67n206
Supporting Variantsnssv17043687
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559355
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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