A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290975



Internal ID20500193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45133726..45133996hg38UCSC Ensembl
chr21:46553641..46553911hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736724
Supporting Variants
Samples
Known GenesADARB1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290975
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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