A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598034



Internal ID20971105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15711433..15904603hg38UCSC Ensembl
chr19:15822243..16015413hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38193171
hg19193171
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3452n223
Supporting Variantsnssv18245800
Samples
Known GenesCYP4F2, CYP4F24P, OR10H1, OR10H2, OR10H3, OR10H5, UCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598034
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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