A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459289



Internal ID21116842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102181345..102183892hg38UCSC Ensembl
chr11:102052076..102054623hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382548
hg192548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178652
Samples
Known GenesYAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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