A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534232



Internal ID20907593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15740705..15815936hg38UCSC Ensembl
chr19:15851515..15926746hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3875232
hg1975232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197658
Samples
Known GenesCYP4F24P, OR10H1, OR10H3, OR10H5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534232
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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