A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855919



Internal ID22630854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69155988..69162663hg38UCSC Ensembl
chr14:69622705..69629380hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg386676
hg196676
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464590
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855919
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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