A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088093



Internal ID21997326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65385997..65385997hg38UCSC Ensembl
chr14:65852715..65852715hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611195
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088093
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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