A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859291



Internal ID22634226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102558714..102560336hg38UCSC Ensembl
chr8:103570942..103572564hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381623
hg191623
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504310
Samples
Known GenesODF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859291
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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