A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246276



Internal ID20813316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40818116..41128657hg38UCSC Ensembl
chr19:41324021..41634562hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38310542
hg19310542
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597631
Supporting Variants
Samples
Known GenesCYP2A13, CYP2A6, CYP2A7, CYP2B6, CYP2B7P, CYP2F1, CYP2G1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246276
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00276


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