A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369430



Internal ID21026983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98498353..98498811hg38UCSC Ensembl
chr3:98217197..98217655hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104930
Samples
Known GenesOR5K2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369430
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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