A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866386



Internal ID22641321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97410727..97415619hg38UCSC Ensembl
chr10:99170484..99175376hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg384893
hg194893
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866386
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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