A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085995



Internal ID21995228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71402661..71402661hg38UCSC Ensembl
chr14:71869378..71869378hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085995
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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