A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495085



Internal ID21152638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21554739..21568814hg38UCSC Ensembl
chr14:22022870..22036945hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3814076
hg1914076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495085
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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