A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474603



Internal ID21132156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102109901..102111900hg38UCSC Ensembl
chr11:101980632..101982631hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191530
Samples
Known GenesYAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474603
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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