A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293961



Internal ID20503179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33563392..33563443hg38UCSC Ensembl
chr21:34935698..34935749hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738429
Supporting Variants
Samples
Known GenesSON
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293961
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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