A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487630



Internal ID21145183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22694413..22716975hg38UCSC Ensembl
chr14:23163622..23186184hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3822563
hg1922563
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487630
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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