A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434111



Internal ID21396113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89482141..89497925hg38UCSC Ensembl
chr3:89531291..89547075hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3815785
hg1915785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15748591
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434111
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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