A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759905



Internal ID20535765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15615910..15615910hg38UCSC Ensembl
chr19:15726721..15726721hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291578
Samples
Known GenesCYP4F8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759905
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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