A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746911



Internal ID20522927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98308156..98308487hg38UCSC Ensembl
chr14:98774493..98774824hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292117
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746911
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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