A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666258



Internal ID21614563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69520282..69541840hg38UCSC Ensembl
chr5:68816109..68837667hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3821559
hg1921559
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151590
Samples
Known GenesOCLN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666258
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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