A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388127



Internal ID21045680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128811001..128813100hg38UCSC Ensembl
chr4:129732156..129734255hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210314
Samples
Known GenesJADE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388127
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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