A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197658



Internal ID20764698
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 StatusS
Merged Variantsnsv6534232
Supporting Variants
Samples
Known GenesCYP4F24P, OR10H1, OR10H3, OR10H5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197658
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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