A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386411



Internal ID21043964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51811201..51896000hg38UCSC Ensembl
chr4:52677367..52762166hg19UCSC Ensembl
Cytoband4q11
Allele length
AssemblyAllele length
hg3884800
hg1984800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5263n223
Supporting Variantsnssv18211885
Samples
Known GenesDCUN1D4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386411
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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