A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493422



Internal ID21150975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27870300..28013405hg38UCSC Ensembl
chr14:28339506..28482611hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38143106
hg19143106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493422
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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