A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445805



Internal ID21103358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8039410..8049346hg38UCSC Ensembl
chr11:8060957..8070893hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg389937
hg199937
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179870
Samples
Known GenesTUB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445805
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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