A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536163



Internal ID311704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38907870..38908035hg38UCSC Ensembl
chr21:40279794..40279959hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726856
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536163
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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