A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379302



Internal ID21036855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70679801..70789100hg38UCSC Ensembl
chr4:71545518..71654817hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38109300
hg19109300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211722
Samples
Known GenesRUFY3, UTP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379302
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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