A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18104288



Internal ID20671328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98264835..98265881hg38UCSC Ensembl
chr3:97983679..97984725hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381047
hg191047
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363240
Supporting Variants
Samples
Known GenesOR5H6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18104288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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