A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739540



Internal ID20515513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35233400..35233452hg38UCSC Ensembl
chr14:35702606..35702658hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278803
Samples
Known GenesKIAA0391
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739540
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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