A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490497



Internal ID21148050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21805301..21896800hg38UCSC Ensembl
chr14:22273473..22364980hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3891500
hg1991508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490497
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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