A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927679



Internal ID22702909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77964983..77966698hg38UCSC Ensembl
chr14:78431326..78433041hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381716
hg191716
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389535
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927679
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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