A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599417



Internal ID20972488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40860603..41136402hg38UCSC Ensembl
chr19:41366508..41642307hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38275800
hg19275800
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3512n223
Supporting Variantsnssv18246279
Samples
Known GenesCYP2A13, CYP2A7, CYP2B6, CYP2B7P, CYP2F1, CYP2G1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599417
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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