A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476364



Internal ID21133917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45459715..45592053hg38UCSC Ensembl
chr14:45928918..46061256hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38132339
hg19132339
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476364
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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