A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085532



Internal ID21994765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72785143..72785143hg38UCSC Ensembl
chr14:73251851..73251851hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg383717
hg193717
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606955
Samples
Known GenesDPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085532
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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