A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047238



Internal ID21956471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15933118..15933315hg38UCSC Ensembl
chr19:16043928..16044125hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619598
Samples
Known GenesCYP4F11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047238
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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