A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759946



Internal ID20535806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99332458..99332458hg38UCSC Ensembl
chr14:99798795..99798795hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759946
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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