A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486589



Internal ID21144142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65267289..65276098hg38UCSC Ensembl
chr14:65734007..65742816hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg388810
hg198810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486589
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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