A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760614



Internal ID20536474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105015386..105015386hg38UCSC Ensembl
chr14:105481723..105481723hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282580
Samples
Known GenesCDCA4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760614
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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