A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485115



Internal ID21142668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49868456..49874272hg38UCSC Ensembl
chr14:50335174..50340990hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg385817
hg195817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485115
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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