A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726780



Internal ID150446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36431260..36432209hg38UCSC Ensembl
chr21:37803558..37804507hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38950
hg19950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541321
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726780
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00281


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