A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434058



Internal ID21396060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43011509..43017508hg38UCSC Ensembl
chr3:43053001..43059000hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753707
SamplesSMI034
Known GenesFAM198A
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434058
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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