A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726833



Internal ID150499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38434559..38436210hg38UCSC Ensembl
chr21:39806481..39808133hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg381652
hg191653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536662
Supporting Variants
Samples
Known GenesERG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726833
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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