A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279519



Internal ID20488737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15707370..15907509hg38UCSC Ensembl
chr19:15818180..16018319hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38200140
hg19200140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740645
Supporting Variants
Samples
Known GenesCYP4F2, CYP4F24P, OR10H1, OR10H2, OR10H3, OR10H5, UCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279519
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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