A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024766



Internal ID21934109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63125994..63133242hg38UCSC Ensembl
chr14:63592712..63599960hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg387249
hg197249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024766
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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