A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485576



Internal ID21143129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53478579..53500479hg38UCSC Ensembl
chr14:53945297..53967197hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3821901
hg1921901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186683
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485576
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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