A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859373



Internal ID22634308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10386086..10390927hg38UCSC Ensembl
chr10:10428049..10432890hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg384842
hg194842
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859373
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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