A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370365



Internal ID21027918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9378301..9458700hg38UCSC Ensembl
chr4:9380027..9460426hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3880400
hg1980400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5172n223
Supporting Variantsnssv18215364
Samples
Known GenesDEFB131
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370365
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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