A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734100



Internal ID157766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15369667..15371371hg38UCSC Ensembl
chr21:16741986..16743690hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530157
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734100
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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