A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986691



Internal ID20553731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110699640..110700116hg38UCSC Ensembl
chr11:110570363..110570839hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465841
Supporting Variants
Samples
Known GenesARHGAP20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00071


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