A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561382



Internal ID334365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110870351..110890481hg38UCSC Ensembl
chr11:110741075..110761205hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3820131
hg1920131
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049243
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561382
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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