A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734452



Internal ID158118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:23722269..23894211hg38UCSC Ensembl
chr21:25094586..25266527hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38171943
hg19171942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527431
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734452
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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