A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204161



Internal ID20771201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45155918..45156550hg38UCSC Ensembl
chr21:46575833..46576465hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544464
Supporting Variants
Samples
Known GenesADARB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204161
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.69529


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