A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734079



Internal ID157745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14884756..14885081hg38UCSC Ensembl
chr21:16257077..16257402hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521221
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734079
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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