A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732819



Internal ID20508745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97787740..97788264hg38UCSC Ensembl
chr14:98254077..98254601hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732819
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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