A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726637



Internal ID150303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32925662..32925739hg38UCSC Ensembl
chr21:34297970..34298047hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545899
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726637
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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