A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597261



Internal ID20970332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15711177..15904597hg38UCSC Ensembl
chr19:15821987..16015407hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38193421
hg19193421
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3452n223
Supporting Variantsnssv18245799
Samples
Known GenesCYP4F2, CYP4F24P, OR10H1, OR10H2, OR10H3, OR10H5, UCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597261
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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