A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393477



Internal ID21051030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170163601..170168100hg38UCSC Ensembl
chr4:171084752..171089251hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393477
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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