A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093783



Internal ID22003016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73828253..73828253hg38UCSC Ensembl
chr14:74294956..74294956hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093783
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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