A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860013



Internal ID22634948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80240169..80245951hg38UCSC Ensembl
chr10:81999925..82005707hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385783
hg195783
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452726, nssv17459566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860013
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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