A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489595



Internal ID21147148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20610218..20610549hg38UCSC Ensembl
chr14:21078377..21078708hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489595
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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