A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985534



Internal ID20552574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100967848..100980618hg38UCSC Ensembl
chr11:100838579..100851349hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3812771
hg1912771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456958
Supporting Variants
Samples
Known GenesARHGAP42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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