A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111184



Internal ID22020417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15933017..15933017hg38UCSC Ensembl
chr19:16043827..16043827hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628406
Samples
Known GenesCYP4F11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111184
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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