A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394824



Internal ID21052377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169902149..169911405hg38UCSC Ensembl
chr4:170823300..170832556hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg389257
hg199257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213871
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394824
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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