A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363240



Internal ID21020793
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 StatusM
Merged Variants
Supporting Variantsnssv18104288
Samples
Known GenesOR5H6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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