A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109718



Internal ID22018951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49701022..49701022hg38UCSC Ensembl
chr19:50204279..50204279hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627050
Samples
Known GenesCPT1C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109718
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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