A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492814



Internal ID21150367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42594770..42649741hg38UCSC Ensembl
chr14:43063973..43118944hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3854972
hg1954972
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187878
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492814
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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