A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480060



Internal ID21137613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22957836..22961138hg38UCSC Ensembl
chr14:23427045..23430347hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383303
hg193303
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480060
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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