A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020514



Internal ID21929857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129143073..129145379hg38UCSC Ensembl
chr11:129012968..129015274hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382307
hg192307
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616025
Samples
Known GenesARHGAP32
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020514
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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