A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734850



Internal ID158516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44088914..44089198hg38UCSC Ensembl
chr21:45508795..45509079hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546868
Supporting Variants
Samples
Known GenesTRAPPC10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734850
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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