A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432411



Internal ID21394413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89089593..89123592hg38UCSC Ensembl
chr16:89156001..89190000hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3834000
hg1934000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750850
SamplesSMI018
Known GenesACSF3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432411
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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