A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599354



Internal ID20972425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40826975..41121253hg38UCSC Ensembl
chr19:41332880..41627158hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38294279
hg19294279
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3512n223
Supporting Variantsnssv18246277
Samples
Known GenesCYP2A13, CYP2A6, CYP2A7, CYP2B6, CYP2B7P, CYP2F1, CYP2G1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599354
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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