A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623686



Internal ID21815733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40880797..40880797hg38UCSC Ensembl
chr19:41386702..41386702hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108559
Supporting Variants
Samples
Known GenesCYP2A7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623686
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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