A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939642



Internal ID22715038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15763126..15763179hg38UCSC Ensembl
chr19:15873936..15873989hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401415
Samples
Known GenesCYP4F24P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939642
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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