A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733756



Internal ID157422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5051386..5051705hg38UCSC Ensembl
chr21:45631850..45632165hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38320
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530688
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733756
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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