A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434216



Internal ID21396218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147094849..147096848hg38UCSC Ensembl
chr4:148016001..148018000hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15748703
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434216
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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