A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734097



Internal ID157763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15216060..15219132hg38UCSC Ensembl
chr21:16588380..16591452hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg383073
hg193073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523013
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734097
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.332969


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