A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442298



Internal ID21099851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4479666..4517334hg38UCSC Ensembl
chr11:4500896..4538564hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3837669
hg1937669
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177964
Samples
Known GenesOR52K1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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