A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484268



Internal ID21141821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:47930035..47987681hg38UCSC Ensembl
chr14:48399238..48456884hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3857647
hg1957647
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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