A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368059



Internal ID21025612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32949269..32958109hg38UCSC Ensembl
chr3:32990761..32999601hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg388841
hg198841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210533
Samples
Known GenesCCR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368059
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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