A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726657



Internal ID150323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33392006..33410684hg38UCSC Ensembl
chr21:34764312..34782990hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3818679
hg1918679
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534026
Supporting Variants
Samples
Known GenesIFNGR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726657
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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