A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383936



Internal ID21041489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67686231..67693562hg38UCSC Ensembl
chr4:68551949..68559280hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg387332
hg197332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211635
Samples
Known GenesUBA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383936
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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