A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859382



Internal ID22634317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41594932..41596980hg38UCSC Ensembl
chr14:42064135..42066183hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382049
hg192049
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859382
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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