A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762734



Internal ID20538594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15708595..15907510hg38UCSC Ensembl
chr19:15819405..16018320hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38198916
hg19198916
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265392
Samples
Known GenesCYP4F2, CYP4F24P, OR10H1, OR10H2, OR10H3, OR10H5, UCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762734
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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