A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386428



Internal ID21043981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64536401..64600500hg38UCSC Ensembl
chr4:65402119..65466218hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3864100
hg1964100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5299n223
Supporting Variantsnssv18211566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386428
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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