A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453822



Internal ID21111375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3084821..3125636hg38UCSC Ensembl
chr11:3106051..3146866hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3840816
hg1940816
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184917
Samples
Known GenesOSBPL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453822
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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