A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487379



Internal ID21144932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82959647..83040969hg38UCSC Ensembl
chr14:83425991..83507313hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3881323
hg1981323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487379
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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