A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859111



Internal ID22634046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132056282..132070090hg38UCSC Ensembl
chr8:133068529..133082337hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3813809
hg1913809
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506888
Samples
Known GenesHHLA1, OC90
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859111
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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