A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471181



Internal ID21128734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108385232..108396253hg38UCSC Ensembl
chr11:108255959..108266980hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3811022
hg1911022
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188009
Samples
Known GenesC11orf65
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471181
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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