A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750374



Internal ID20526389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6429032..6429032hg38UCSC Ensembl
chr19:6429043..6429043hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275899
Samples
Known GenesSLC25A41
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750374
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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