A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748769



Internal ID21392281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38083510..38085509hg38UCSC Ensembl
chr3:38125001..38127000hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434052
Supporting Variants
SamplesSMI034
Known GenesDLEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748769
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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