A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855634



Internal ID22630569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80269454..80276447hg38UCSC Ensembl
chr8:81181689..81188682hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg386994
hg196994
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855634
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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