A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291831



Internal ID20501049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110648166..110648235hg38UCSC Ensembl
chr11:110518889..110518958hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738178
Supporting Variants
Samples
Known GenesARHGAP20
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291831
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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