A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445828



Internal ID22112005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105015398..105015398hg38UCSC Ensembl
chr14:105481735..105481735hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767147
Samples
Known GenesCDCA4
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445828
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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