A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494617



Internal ID21152170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20721855..20729781hg38UCSC Ensembl
chr14:21190014..21197940hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg387927
hg197927
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494617
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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