A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380460



Internal ID21038013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16393831..16447953hg38UCSC Ensembl
chr5:16393940..16448062hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3854123
hg1954123
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215963
Samples
Known GenesLOC101929505
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380460
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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