A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726398



Internal ID150064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26145549..26150110hg38UCSC Ensembl
chr21:27517867..27522428hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg384562
hg194562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520430
Supporting Variants
Samples
Known GenesAPP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726398
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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